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1,4-Diazepino[6,5-b]indol-2(1H)-one, 1-(4-ethoxyphenyl)-3,6-dihydro-, 4-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

658041-41-9

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658041-41-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 658041-41-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,8,0,4 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 658041-41:
(8*6)+(7*5)+(6*8)+(5*0)+(4*4)+(3*1)+(2*4)+(1*1)=159
159 % 10 = 9
So 658041-41-9 is a valid CAS Registry Number.

658041-41-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-ethoxyphenyl)-2-oxo-1,2,3,6-tetrahydro[1,4]diazepino[6,5-b]indole 4-oxide

1.2 Other means of identification

Product number -
Other names 1-(4-Ethoxy-phenyl)-4-oxy-3,6-dihydro-1H-[1,4]diazepino[6,5-b]indol-2-one

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:658041-41-9 SDS

658041-41-9Downstream Products

658041-41-9Relevant academic research and scientific papers

Synthesis and study of some properties of 1-aryl-2-oxo-1,2,3,6- tetrahydro[1,4]diazepino[6,5-b]indole 4-oxides

Ryabova,Rastorgueva,Lisitsa,Alekseeva,Granik

, p. 1386 - 1398 (2007/10/03)

A number of 1-aryl-2-oxo-1,2,3,6-tetrahydro[1,4]diazepirio[6,5-b]indole 4-oxides were synthesized based on 3-[N-aryl-N-(chloroacetyl)amino]-2- formylindoles. The nature of the substituent in the 1-aryl fragment has a pronounced influence on the course of reactions throughout the whole sequence of transformations during the synthesis of diazepinoindoles. The reduction of 4-oxides by formamidinosulfinic acid, hydrogen in the presence of Pd/C, and sodium bisulfite was studied. The structures of the reaction products were confirmed using IR and 1H NMR spectroscopy and mass spectrometry.

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