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L-Tryptophan, N-[[2-[(2,6-dichlorophenyl)amino]phenyl]acetyl]-, hydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

192377-11-0

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192377-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 192377-11-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,3,7 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 192377-11:
(8*1)+(7*9)+(6*2)+(5*3)+(4*7)+(3*7)+(2*1)+(1*1)=150
150 % 10 = 0
So 192377-11-0 is a valid CAS Registry Number.

192377-11-0SDS

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 2-[2-(2,6-Dichloro-phenylamino)-phenyl]-N-[(S)-1-hydrazinocarbonyl-2-(1H-indol-3-yl)-ethyl]-acetamide

1.2 Other means of identification

Product number -
Other names -

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:192377-11-0 SDS

192377-11-0Downstream Products

192377-11-0Relevant academic research and scientific papers

Studies on o-[2,6-dichlorophenyl-1-amino] phenyl acetic acid I. Synthesis, antiinflammatory, analgesic and ulcerogenic activities of some new amino acid conjugates

Shalaby,El-Eraky

, p. 83 - 87 (2007/10/03)

o-[2,6-Dichlorophenyl-1-amino]phenyl acetic acid (diclofenac) (I) reacted with some amino-acid esters, namely glycine, L-valine, L- diiodotyrosine and L-tryptophan through the active ester to give the corresponding o-[2,6-dichlorophenyl-1-amino]benzyl carboxy-N-amino acid ester of the type (IIa-d), respectively, which were hydrolysed in alkaline medium to yield the free amino acids (IIIa-d). Condensation of the latter compounds with hydrazine hydrate gave the corresponding acid hydrazides (IVa-d), which in turn were reacted with trimethoxybenzaldehyde to give the corresponding Schiff's bases (Va-d), respectively. The antiinflammatory, ulcerogenic and analgesic activities of the obtained compounds were also investigated.

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