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C-(2'-METHOXY-BIPHENYL-4-YL)-METHYLAMINE HYDROCHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

858674-01-8

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858674-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 858674-01-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,8,6,7 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 858674-01:
(8*8)+(7*5)+(6*8)+(5*6)+(4*7)+(3*4)+(2*0)+(1*1)=218
218 % 10 = 8
So 858674-01-8 is a valid CAS Registry Number.

858674-01-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name C-(2'-METHOXY-BIPHENYL-4-YL)-METHYLAMINE HYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names 3-Aminomethyl-2-methoxy-4,6-dimethylpyridin

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:858674-01-8 SDS

858674-01-8Relevant academic research and scientific papers

Compounds with medicinal effects due to interaction with the glucocorticoid receptor

-

Page/Page column 8, (2010/11/27)

The invention provides for compounds having the structure according to the formula I

Novel series of substituted biphenylmethyl urea derivatives as MCH-R1 antagonists for the treatment of obesity

Galiano, Silvia,Ceras, Javier,Cirauqui, Nuria,Perez, Silvia,Juanenea, Laura,Rivera, Gildardo,Aldana, Ignacio,Monge, Antonio

, p. 3896 - 3911 (2008/02/11)

We have designed and synthesized two novel series of MCH-R1 antagonists based on a substituted biphenylmethyl urea core. SAR was explored, suggesting that optimal binding with the receptor was achieved when the biphenylmethyl group and the linker were sub

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