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GB929395A - - Google Patents

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Publication number
GB929395A
GB929395A GB91363A GB91363A GB929395A GB 929395 A GB929395 A GB 929395A GB 91363 A GB91363 A GB 91363A GB 91363 A GB91363 A GB 91363A GB 929395 A GB929395 A GB 929395A
Authority
GB
United Kingdom
Prior art keywords
pyrazolone
alkyl
residue
acid
carbalkoxy
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
GB91363A
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.)
Bayer AG
Original Assignee
Bayer AG
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
Application filed by Bayer AG filed Critical Bayer AG
Priority to GB91363A priority Critical patent/GB929395A/en
Publication of GB929395A publication Critical patent/GB929395A/en
Expired legal-status Critical Current

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Abstract

The Specification relates to methine dyes of the general formula:- <FORM:0929395/IV(a)/1> wherein R2 is a carbalkoxy group, R3 is hydrogen or alkyl and R5 is the residue of a 5-pyrazolone, cyanacetic acid or an alkyl ester, substituted alkyl ester or amide thereof, or of malonic acid dinitrile, the residue R5 being free from sulphonic acid groups and all the said alkyl and alkoxy groups containing from 1 to 5 carbon atoms. The dyes are prepared by condensing a compound R5H2 with a 3;3-dimethyl-5-carbalkoxy-2-methylene indoline-o -aldehyde, preferably in an alkaline medium. An emulsifying agent such as polyoxyethylene oleyl ether also may be present. In the case where R5 is the residue of a 5-pyrazolone, the dyes may be prepared by reacting a 3;3-dimethyl-5-carbalkoxy-2-methyleneindoline with a 5-pyrazolone having in its 4-position a -CHO or =CH-N(alkyl)2 group, preferably in the presence of an acid. Pyrazolone components are specified having a 1-phenyl, chlorophenyl, dichlorophenyl, nitrophenyl, aminophenyl, acetylaminophenyl, carboxyphenyl or methyl-phenyl substituent and a 3-methyl or carboxylic acid ester or amide substituent. Specification 929,394 also is referred to.
GB91363A 1959-08-21 1959-08-21 Expired GB929395A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB91363A GB929395A (en) 1959-08-21 1959-08-21

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB91363A GB929395A (en) 1959-08-21 1959-08-21

Publications (1)

Publication Number Publication Date
GB929395A true GB929395A (en) 1963-06-19

Family

ID=9712711

Family Applications (1)

Application Number Title Priority Date Filing Date
GB91363A Expired GB929395A (en) 1959-08-21 1959-08-21

Country Status (1)

Country Link
GB (1) GB929395A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5136045A (en) * 1989-09-22 1992-08-04 Sumitomo Chemical Company, Limited Pyrazole containing methine compounds

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5136045A (en) * 1989-09-22 1992-08-04 Sumitomo Chemical Company, Limited Pyrazole containing methine compounds

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