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Pyrido[1,2-a][1,4]diazepine, decahydro-2-methyl-4-nitro-4-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62176-08-3

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62176-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62176-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,7 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62176-08:
(7*6)+(6*2)+(5*1)+(4*7)+(3*6)+(2*0)+(1*8)=113
113 % 10 = 3
So 62176-08-3 is a valid CAS Registry Number.

62176-08-3SDS

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 4-benzyl-2-methyl-4-nitro-decahydro-pyrido[1,2-a][1,4]diazepine

1.2 Other means of identification

Product number -
Other names 4-Benzyl-2-methyl-4-nitroperhydropyrido[1,2-a][1,4]-diazepine

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:62176-08-3 SDS

62176-08-3Upstream product

62176-08-3Downstream Products

62176-08-3Relevant academic research and scientific papers

4-Nitroperhydropyrido[1,2-a][1,4]diazepines

-

, (2008/06/13)

Compounds of the formula v,2/12 Wherein R1 is H, lower-alkyl, hydroxyalkyl, phenyl, aralkyl, or --(CH2) n --X wherein n is 0-4 and X is --COO-lower-alkyl, C N or --COOH and R2 is H, lower-alkyl or aralkyl, produced by condensing a diamine of the formula SPC1 With a nitro compound of the formula R1 --CH2 --NO2 in the presence of formalin or paraformaldehyde, or with the R1 -- C(CH2 OH)2 NO2 reaction product of the above nitro compound and formalin or paraformaldehyde, or with formalin or paraformaldehyde followed by reaction with the above nitro compound, and their acid addition salts, possess antimicrobial activity against both gram-positive and gram-negative bacteria and also against dermatophytes, yeasts and other fungi.

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