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1131623-15-8

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1131623-15-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1131623-15-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,1,6,2 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1131623-15:
(9*1)+(8*1)+(7*3)+(6*1)+(5*6)+(4*2)+(3*3)+(2*1)+(1*5)=98
98 % 10 = 8
So 1131623-15-8 is a valid CAS Registry Number.

1131623-15-8SDS

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-Amino-5-hydroxy-2-(trifluoromethyl)benzonitrile

1.2 Other means of identification

Product number -
Other names I01-8771

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:1131623-15-8 SDS

1131623-15-8Downstream Products

1131623-15-8Relevant articles and documents

Structural elucidation of major selective androgen receptor modulator (SARM) metabolites for doping control

Garg, Neeraj,Hansson, Annelie,Knych, Heather K.,Stanley, Scott D.,Thevis, Mario,Bondesson, Ulf,Hedeland, Mikael,Globisch, Daniel

, p. 698 - 702 (2018)

Selective androgen receptor modulators (SARMs) are a class of androgen receptor drugs, which have a high potential to be performance enhancers in human and animal sports. Arylpropionamides are one of the major SARM classes and get rapidly metabolized significantly complicating simple detection of misconduct in blood or urine sample analysis. Specific drug-derived metabolites are required as references due to a short half-life of the parent compound but are generally lacking. The difficulty in metabolism studies is the determination of the correct regio and stereoselectivity during metabolic conversion processes. In this study, we have elucidated and verified the chemical structure of two major equine arylpropionamide-based SARM metabolites using a combination of chemical synthesis and liquid chromatography-mass spectrometry (LC-MS) analysis. These synthesized SARM-derived metabolites can readily be utilized as reference standards for routine mass spectrometry-based doping control analysis of at least three commonly used performance-enhancing drugs to unambigously identify misconduct.

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