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756477-41-5

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756477-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 756477-41-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,6,4,7 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 756477-41:
(8*7)+(7*5)+(6*6)+(5*4)+(4*7)+(3*7)+(2*4)+(1*1)=205
205 % 10 = 5
So 756477-41-5 is a valid CAS Registry Number.

756477-41-5SDS

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 2-methylthieno[2,3-c]pyridine

1.2 Other means of identification

Product number -
Other names 2-Methyl-thieno[2,3-c]pyridine

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:756477-41-5 SDS

756477-41-5Relevant articles and documents

THIENOPYRIDYL COMPOUNDS THAT INHIBIT VANILLOID RECEPTOR SUBTYPE 1 (VR1) AND USES THEREOF

-

Page/Page column 24, (2008/06/13)

The present invention discloses fused thienopyridyl compounds of general formula (I), wherein X1-X6, R5-R7, Z1 and L are as defined in the description. The resent invention also discloses a method for

A rapid synthesis of thieno[2,3-c]pyridine and 2-substituted thieno[2,3-c]pyridines

Graulich, Amaury,Liegeois, Jean-Francois

, p. 1935 - 1937 (2007/10/03)

A convenient preparation of thieno[2,3-c]pyridine 3a and of several original 2-substituted-thieno[2,3-c]pyridines 3b-f is achieved by cyclization of the Schiff base resulting from the condensation between a 2- thiophenecarboxaldehyde 1a-f and aminoacetaldehyde dimethyl acetal. This procedure provides especially good yields in the case of 2-halogenated analogues.

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