GB1497000A - Fluorescent dyes - Google Patents
Fluorescent dyesInfo
- Publication number
- GB1497000A GB1497000A GB1617176A GB1617176A GB1497000A GB 1497000 A GB1497000 A GB 1497000A GB 1617176 A GB1617176 A GB 1617176A GB 1617176 A GB1617176 A GB 1617176A GB 1497000 A GB1497000 A GB 1497000A
- Authority
- GB
- United Kingdom
- Prior art keywords
- additionally
- general formula
- fluorescent dyes
- april
- nitrogen
- Prior art date
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D277/70—Sulfur atoms
- C07D277/74—Sulfur atoms substituted by carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D235/28—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B3/00—Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
- C09B3/02—Benzathrones
- C09B3/06—Preparation from starting materials already containing the benzanthrone nucleus
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/02—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic ring being only condensed in peri position
- C09B5/14—Benz-azabenzanthrones (anthrapyridones)
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
1497000 Fluorescent dyes MONTEDISON SpA 21 April 1976 [24 April 1975 (2)] 16171/76 Heading C4P The invention comprises fluorescent dyes having the general formula wherein Z is a nitrogen or carbon atom, X is H or is additionally bromine when Z is carbon, Y is methoxy or ethoxy or is additionally H when Z is a carbon atom, and X' is -NH- or additionally -S- when Z is nitrogen. They are prepared by reacting a halogen substituted compound of the general formula wherein X, Y and Z are as above and A is Cl or Br with a compound of the general formula wherein X' is as above in an aprotic dipolar solvent at 80-140‹ C. in presence of an acid acceptor. The solvents include dimethylformamide, dimethylacetamide, dimethylsulphoxide, 1-methylpyrrolidin-2-one, hexamethylphosphotriamide and mixtures thereof. Acid acceptors used are sodium and potassium carbonates, pyridine and piperidine. The dyes are used to bulk dye polystyrene, polymethylmethacrylate, rigid P.V.C. polyethylene, acrylonitrile-butadiene-styrene copolymers and polycarbonates, and to colour mineral oils.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT22722/75A IT1037620B (en) | 1975-04-24 | 1975-04-24 | FLUORESCENT BENZANTRON DYES |
IT22723/75A IT1037621B (en) | 1975-04-24 | 1975-04-24 | FLUORESCENT AZABENZANTRONIC DYES |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1497000A true GB1497000A (en) | 1978-01-05 |
Family
ID=26328249
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1617176A Expired GB1497000A (en) | 1975-04-24 | 1976-04-21 | Fluorescent dyes |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1497000A (en) |
-
1976
- 1976-04-21 GB GB1617176A patent/GB1497000A/en not_active Expired
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |