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1H-Inden-1-one,2-amino-2,3-dihydro-4,5,6,7-tetramethyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

780743-34-2

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780743-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 780743-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,0,7,4 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 780743-34:
(8*7)+(7*8)+(6*0)+(5*7)+(4*4)+(3*3)+(2*3)+(1*4)=182
182 % 10 = 2
So 780743-34-2 is a valid CAS Registry Number.

780743-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-4,5,6,7-tetramethyl-1-indanone

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:780743-34-2 SDS

780743-34-2Relevant academic research and scientific papers

An investigation into the structure-activity relationships associated with the systematic modification of the β2-adrenoceptor agonist indacaterol

Beattie, David,Beer, David,Bradley, Michelle E.,Bruce, Ian,Charlton, Steven J.,Cuenoud, Bernard M.,Fairhurst, Robin A.,Farr, David,Fozard, John R.,Janus, Diana,Rosethorne, Elizabeth M.,Sandham, David A.,Sykes, David A.,Trifilieff, Alexandre,Turner, Katharine L.,Wissler, Elke

, p. 6280 - 6285 (2012/10/30)

The synthesis of a series of indacaterol analogues in which each of the three structural regions of indacaterol are modified in a systematic manner is described. Evaluation of the affinity of these analogues for the β2-adrenoceptor identified t

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