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3H-Benzo[d][1,2,3]triazol-5-aMine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

503183-58-2

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503183-58-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 503183-58-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,1,8 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 503183-58:
(8*5)+(7*0)+(6*3)+(5*1)+(4*8)+(3*3)+(2*5)+(1*8)=122
122 % 10 = 2
So 503183-58-2 is a valid CAS Registry Number.

503183-58-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-aminobenzotriazole

1.2 Other means of identification

Product number -
Other names 2H-benzotriazol-5-ylamine

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:503183-58-2 SDS

503183-58-2Upstream product

503183-58-2Downstream Products

503183-58-2Relevant academic research and scientific papers

Pyrazole compounds

-

, (2008/06/13)

Pharmaceutical compositions and compounds are provided. The compounds of the invention demonstrate anti-proliferative activity, and may promote apoptosis in cells lacking normal regulation of cell cycle and death. In one embodiment of the invention, pharmaceutical compositions of the compounds in combination with a physiologically acceptable carrier are provided. The pharmaceutical compositions are useful in the treatment of hyperproliferative disorders, which disorders include tumor growth, lymphoproliferative diseases, angiogenesis. The compounds of the invention are substituted pyrazoles and pyrazolines.

Addition reactions of 5-aminobenzotriazoles with dimethyl acetylenedicarboxylate (DMAD). Formation of (Z/E) Michael adducts, (benzotriazol-5-yl)-2-pyridones, a triazolo-9,10-dihydrobenzoazepine and a triazolo-2-oxindole

Sanna, Paolo,Nuvole, Antonio,Sequi, Piera Attilia,Paglietti, Giuseppe

, p. 259 - 280 (2007/10/02)

5-Aminobenzotriazoles (1a-d) reacted with DMAD to give the regioselective Michael adducts (Z)-(2a-d), accompanied with (benzotriazol-5-yl)-2-pyridones (3b-d), and in one case (2c) with the triazolo-9,10-dihydrobenzoazepine (4).Cyclisation of the adducts (Z)-(2b-d) in Dowtherm gave the triazoloquinolinones (6b-d), which were converted into chloro derivatives (9b-d), in turn hydrolysed and decarboxylated to 9-chloro-1(2)-methyltriazoloquinolines (11c-d).Compound (1c) in refluxing acetonitrile with DMAD undergoes unusual cyclisation into triazolo-2-oxindole (5), then converted into 2-methyltriazolocarbostyril-9-carboxylate (17).

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