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1H-Pyrrol-3-ol, 2,3-dihydro-2-imino-4-methyl-3-(4-nitrophenyl)-5-phenyl-1-(phenylmethyl )- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88875-52-9

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88875-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88875-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,8,7 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88875-52:
(7*8)+(6*8)+(5*8)+(4*7)+(3*5)+(2*5)+(1*2)=199
199 % 10 = 9
So 88875-52-9 is a valid CAS Registry Number.

88875-52-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-4-hydroxy-5-imino-3-methyl-4-(4-nitrophenyl)-2-phenyl-4,5-dihydropyrrole

1.2 Other means of identification

Product number -
Other names 1-Benzyl-2-imino-4-methyl-3-(4-nitro-phenyl)-5-phenyl-2,3-dihydro-1H-pyrrol-3-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88875-52-9 SDS

88875-52-9Relevant academic research and scientific papers

Reaction of N-(1-Phenylalkylidene)benzylamines with Benzoyl Cyanides

Sakamoto, Masanori,Akiyama, Yasunobu,Furumi, Nobuko,Ishii, Keitaro,Tomimatsu, Yoshio,Date, Tadamasa

, p. 2623 - 2631 (2007/10/02)

Reactions of variuos aldimines 4a-f with 4-nitrobenzoyl cyanide (2b) gave the Reissert-type compounds 5a-f.However, reaction of N-(1-phenylpropylidene)benzylamine (7a) with 2b gave 1-benzyl-4-hydroxy-5-imino-3-methyl-4-(4-nitrophenyl)-2-phenyl-4,5-dihydropyrrole (8a).Similar reactions of 7b, 7c, and 12 with 2b gave the pyrrole derivatives 8b, 11, and 13, respectively.Next, the reaction of N-cyclohexylidenecyclohexylamine (14) with benzoyl cyanide (2a) was reexamined.The structure of the adduct 16 was different from that of the Reissert-type compound 15 described by Dornow and Luepfert.Keywords - Reissert reaction; benzoyl cyanide; 4-nitrobenzoyl cyanide; aldimine; ketimine; X-ray analysis; dihydropyrrole; cyclization

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