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ethyl 1-{4-nitrophenyl}-2-methyl-1H-pyrido[3,2-b]indole-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

374697-64-0

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374697-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 374697-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,4,6,9 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 374697-64:
(8*3)+(7*7)+(6*4)+(5*6)+(4*9)+(3*7)+(2*6)+(1*4)=200
200 % 10 = 0
So 374697-64-0 is a valid CAS Registry Number.

374697-64-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-3-ethoxycarbonyl-2-methyl-1-(p-nitrophenyl)pyrido[3,2-b]indole

1.2 Other means of identification

Product number -
Other names 1H-2-methyl-1-p-nitrophenyl-3-ethoxycarbonylpyrido[3,2-b]indole

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:374697-64-0 SDS

374697-64-0Upstream product

374697-64-0Relevant academic research and scientific papers

Synthesis and some transformations of derivatives of pyrido-[3,2-b]indole (δ-carboline)

Ryabova,Alekseeva,Granik

, p. 997 - 1004 (2007/10/03)

The reactions of 2-dimethyliminomethyl-3-(p-nitrophenyl)aminoindole chloride with compounds with an active methylene center have been studied. A series of derivatives of δ-carboline have been synthesized. By the reaction of 3-ethoxycarbonyl-2-methyl-l-p-nitrophenylpyrido[3,2-b]indolinium chloride with the diethyl acetal of DMF the corresponding 2-dimethylaminovinyl derivative was synthesized which was converted into 5-p-nitrophenyl-1-oxo-1,10-dihydropyrano [3′,4′:5,6]pyrido[3,2-b]indol-5-ium chloride in the presence of acid.

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