GB1375270A

GB1375270A – – Google Patents

GB1375270A – – Google Patents

Info

Publication number
GB1375270A

GB1375270A
GB2901472A
GB2901472A
GB1375270A
GB 1375270 A
GB1375270 A
GB 1375270A
GB 2901472 A
GB2901472 A
GB 2901472A
GB 2901472 A
GB2901472 A
GB 2901472A
GB 1375270 A
GB1375270 A
GB 1375270A
Authority
GB
United Kingdom
Prior art keywords
formula
compound
hydrogen
reacting
optionally substituted
Prior art date
1971-06-23
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Expired

Application number
GB2901472A
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
1971-06-23
Filing date
1972-06-21
Publication date
1974-11-27

1971-06-23
Priority claimed from CH916671A
external-priority
patent/CH564045A5/xx

1972-06-21
Application filed
filed
Critical

1974-11-27
Publication of GB1375270A
publication
Critical
patent/GB1375270A/en

Status
Expired
legal-status
Critical
Current

Links

Espacenet

Global Dossier

Discuss

150000001875
compounds
Chemical class

0.000
abstract
12

229910052739
hydrogen
Inorganic materials

0.000
abstract
7

239000001257
hydrogen
Substances

0.000
abstract
7

NAWXUBYGYWOOIX-SFHVURJKSA-N
(2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid
Chemical compound

C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1
NAWXUBYGYWOOIX-SFHVURJKSA-N
0.000
abstract
5

125000000547
substituted alkyl group
Chemical group

0.000
abstract
5

125000003342
alkenyl group
Chemical group

0.000
abstract
3

150000002431
hydrogen
Chemical class

0.000
abstract
3

125000002887
hydroxy group
Chemical group

[H]O*

0.000
abstract
3

125000001997
phenyl group
Chemical group

[H]C1=C([H])C([H])=C(*)C([H])=C1[H]

0.000
abstract
3

UFHFLCQGNIYNRP-UHFFFAOYSA-N
Hydrogen
Chemical compound

[H][H]
UFHFLCQGNIYNRP-UHFFFAOYSA-N
0.000
abstract
2

125000003545
alkoxy group
Chemical group

0.000
abstract
2

-1
aralkoxy
Chemical group

0.000
abstract
2

125000000753
cycloalkyl group
Chemical group

0.000
abstract
2

150000005690
diesters
Chemical class

0.000
abstract
2

229910052736
halogen
Inorganic materials

0.000
abstract
2

150000002367
halogens
Chemical group

0.000
abstract
2

125000004435
hydrogen atom
Chemical group

[H]*

0.000
abstract
2

235000011149
sulphuric acid
Nutrition

0.000
abstract
2

239000001117
sulphuric acid
Substances

0.000
abstract
2

239000004215
Carbon black (E152)
Substances

0.000
abstract
1

ISWSIDIOOBJBQZ-UHFFFAOYSA-N
Phenol
Chemical compound

OC1=CC=CC=C1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N
0.000
abstract
1

QAOWNCQODCNURD-UHFFFAOYSA-N
Sulfuric acid
Chemical compound

OS(O)(=O)=O
QAOWNCQODCNURD-UHFFFAOYSA-N
0.000
abstract
1

239000002253
acid
Substances

0.000
abstract
1

150000007513
acids
Chemical class

0.000
abstract
1

125000003302
alkenyloxy group
Chemical group

0.000
abstract
1

125000004448
alkyl carbonyl group
Chemical group

0.000
abstract
1

125000004390
alkyl sulfonyl group
Chemical group

0.000
abstract
1

125000003118
aryl group
Chemical group

0.000
abstract
1

239000003795
chemical substances by application
Substances

0.000
abstract
1

125000000000
cycloalkoxy group
Chemical group

0.000
abstract
1

229940042400
direct acting antivirals phosphonic acid derivative
Drugs

0.000
abstract
1

150000002148
esters
Chemical class

0.000
abstract
1

125000005843
halogen group
Chemical group

0.000
abstract
1

229930195733
hydrocarbon
Natural products

0.000
abstract
1

230000003301
hydrolyzing effect
Effects

0.000
abstract
1

239000000463
material
Substances

0.000
abstract
1

125000000951
phenoxy group
Chemical group

[H]C1=C([H])C([H])=C(O*)C([H])=C1[H]

0.000
abstract
1

150000003007
phosphonic acid derivatives
Chemical class

0.000
abstract
1

230000005855
radiation
Effects

0.000
abstract
1

150000003839
salts
Chemical class

0.000
abstract
1

239000003381
stabilizer
Substances

0.000
abstract
1

125000001424
substituent group
Chemical group

0.000
abstract
1

238000005809
transesterification reaction
Methods

0.000
abstract
1

Classifications

A—HUMAN NECESSITIES

A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE

A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS

A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings

A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations

A—HUMAN NECESSITIES

A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE

A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES

A61K8/00—Cosmetics or similar toiletry preparations

A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition

A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds

A61K8/55—Phosphorus compounds

C—CHEMISTRY; METALLURGY

C07—ORGANIC CHEMISTRY

C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM

C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System

C07F9/02—Phosphorus compounds

C07F9/28—Phosphorus compounds with one or more P—C bonds

C07F9/38—Phosphonic acids RP(=O)(OH)2; Thiophosphonic acids, i.e. RP(=X)(XH)2 (X = S, Se)

C07F9/40—Esters thereof

C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic

C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl

C—CHEMISTRY; METALLURGY

C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON

C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients

C08K5/00—Use of organic ingredients

C08K5/49—Phosphorus-containing compounds

C08K5/51—Phosphorus bound to oxygen

C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only

C08K5/5317—Phosphonic compounds, e.g. R—P(:O)(OR’)2

C08K5/5333—Esters of phosphonic acids

D—TEXTILES; PAPER

D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR

D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS

D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment

D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen

D06M13/152—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen having a hydroxy group bound to a carbon atom of a six-membered aromatic ring

G—PHYSICS

G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY

G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY

G03C1/00—Photosensitive materials

G03C1/76—Photosensitive materials characterised by the base or auxiliary layers

G03C1/815—Photosensitive materials characterised by the base or auxiliary layers characterised by means for filtering or absorbing ultraviolet light, e.g. optical bleaching

G03C1/8155—Organic compounds therefor

G—PHYSICS

G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY

G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY

G03C11/00—Auxiliary processes in photography

G03C11/08—Varnishing, e.g. application of protective layers on finished photographic prints

G03C11/10—Varnishing, e.g. application of protective layers on finished photographic prints for protection from ultraviolet light

H—ELECTRICITY

H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR

H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS

H05K2203/00—Indexing scheme relating to apparatus or processes for manufacturing printed circuits covered by H05K3/00

H05K2203/01—Tools for processing; Objects used during processing

H05K2203/0147—Carriers and holders

H05K2203/0152—Temporary metallic carrier, e.g. for transferring material

H—ELECTRICITY

H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR

H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS

H05K2203/00—Indexing scheme relating to apparatus or processes for manufacturing printed circuits covered by H05K3/00

H05K2203/07—Treatments involving liquids, e.g. plating, rinsing

H05K2203/0703—Plating

H05K2203/0726—Electroforming, i.e. electroplating on a metallic carrier thereby forming a self-supporting structure

Abstract

1375270 Phosphonic acid derivatives CIBAGEIGY AG 21 June 1972 [23 June 1971] 29014/72 Heading C2P [Also in Division G2] Compounds of Formula I where A is a hydrocarbon radical, D and D1 are either both hydrogen, cycloalkyl, alkenyl or optionally substituted alkyl or phenyl or one is hydrogen and the other is cycloalkyl, alkenyl or optionally substituted alkyl or phenyl, X is hydrogen, halogen, hydroxyl, alkenyl, alkylcarbonyl, alkylsulphonyl, alkoxy, alkenyloxy, cycloalkoxy, aralkoxy, phenoxy, optionally substituted alkyl or phenyl or a radical of Formula (i) Y and Z are hydrogen, halogen, hydroxyl or optionally substituted alkyl or alkoxy and R is hydrogen or a radical of Formula II, and salts thereof when at least one of D and D1 is hydrogen and alcoholates thereof when at least one OH is present as a substituent, which compounds are used as stabilizers against ultraviolet radiation for photographic materials, may be prepared (a) by reacting a phenol of Formula (10) with a compound of Formula (11) or with a sulphuric acid mono- or diester thereof, or by reacting a sulphuric acid ester of the compound of Formula (10) with a compound of Formula (11) or (b) by reacting a compound of Formula (10) with a compound of Formula (12) or (c) by reacting a compound of Formula (10) with a compound of Formula (18) where E11 is a halogen atom or a group -SO 3 E1 where E1 is optionally substituted alkyl or aryl or (d) reacting a compound of Formula (10) in which one or both OH groups is/are replaced by E11 with a compound of Formula (11). Compounds of Formula I in which D and D1 are hydrogen may be prepared by hydrolysing mono- or diesters of Formula I, and esters of Formula I may be obtained by esterifying the free acids or by transesterification.

GB2901472A
1971-06-23
1972-06-21

Expired

GB1375270A
(en)

Applications Claiming Priority (1)

Application Number
Priority Date
Filing Date
Title

CH916671A

CH564045A5
(en)

1970-06-24
1971-06-23

Publications (1)

Publication Number
Publication Date

GB1375270A
true

GB1375270A
(en)

1974-11-27

Family
ID=4349059
Family Applications (1)

Application Number
Title
Priority Date
Filing Date

GB2901472A
Expired

GB1375270A
(en)

1971-06-23
1972-06-21

Country Status (7)

Country
Link

BE
(1)

BE785253A
(en)

CA
(1)

CA995955A
(en)

CH
(1)

CH558203A
(en)

DE
(1)

DE2230301A1
(en)

FR
(1)

FR2142987B1
(en)

GB
(1)

GB1375270A
(en)

IT
(1)

IT958458B
(en)

Cited By (2)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

WO2002048118A1
(en)

*

2000-12-12
2002-06-20
Ciba Specialty Chemicals Holding Inc.
Benzophenone uv-absorbers with heterocyclic substituents

US8529877B2
(en)

2008-11-13
2013-09-10
Basf Se
Benzylidene compounds comprising phosphono-groups

1971

1971-06-23
CH
CH916671A
patent/CH558203A/en
not_active
IP Right Cessation

1972

1972-06-12
FR
FR7221087A
patent/FR2142987B1/fr
not_active
Expired

1972-06-15
CA
CA144,781A
patent/CA995955A/en
not_active
Expired

1972-06-21
DE
DE19722230301
patent/DE2230301A1/en
active
Pending

1972-06-21
GB
GB2901472A
patent/GB1375270A/en
not_active
Expired

1972-06-21
IT
IT5103072A
patent/IT958458B/en
active

1972-06-22
BE
BE785253A
patent/BE785253A/en
unknown

Cited By (2)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

WO2002048118A1
(en)

*

2000-12-12
2002-06-20
Ciba Specialty Chemicals Holding Inc.
Benzophenone uv-absorbers with heterocyclic substituents

US8529877B2
(en)

2008-11-13
2013-09-10
Basf Se
Benzylidene compounds comprising phosphono-groups

Also Published As

Publication number
Publication date

BE785253A
(en)

1972-12-22

FR2142987A1
(en)

1973-02-02

FR2142987B1
(en)

1978-03-03

IT958458B
(en)

1973-10-20

DE2230301A1
(en)

1972-12-28

CA995955A
(en)

1976-08-31

CH558203A
(en)

1975-01-31

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Legal Events

Date
Code
Title
Description

1975-04-09
PS
Patent sealed

1983-01-26
PCNP
Patent ceased through non-payment of renewal fee

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