GB1497000A - Fluorescent dyes - Google Patents

Fluorescent dyes

Info

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
Application number
GB1617176A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Montedison SpA
Original Assignee
Montedison SpA
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.)
Filing date
Publication date
Priority claimed from IT22722/75A external-priority patent/IT1037620B/en
Priority claimed from IT22723/75A external-priority patent/IT1037621B/en
Application filed by Montedison SpA filed Critical Montedison SpA
Publication of GB1497000A publication Critical patent/GB1497000A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/60Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D277/62Benzothiazoles
    • C07D277/68Benzothiazoles 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
    • C07D277/70Sulfur atoms
    • C07D277/74Sulfur atoms substituted by carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/24Benzimidazoles; 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
    • C07D235/28Sulfur atoms
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B3/00Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
    • C09B3/02Benzathrones
    • C09B3/06Preparation from starting materials already containing the benzanthrone nucleus
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B5/00Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
    • C09B5/02Dyes 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
    • C09B5/14Benz-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.
GB1617176A 1975-04-24 1976-04-21 Fluorescent dyes Expired GB1497000A (en)

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)

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee