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53885-53-3

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53885-53-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53885-53-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,8 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 53885-53:
(7*5)+(6*3)+(5*8)+(4*8)+(3*5)+(2*5)+(1*3)=153
153 % 10 = 3
So 53885-53-3 is a valid CAS Registry Number.

53885-53-3SDS

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 5-[(2-methylphenyl)methyl]-6,7-dihydro-4H-thieno[3,2-c]pyridine,hydrochloride

1.2 Other means of identification

Product number -
Other names 5-(2-methylbenzyl)-4,5,6,7-tetrahydro-thieno[3,2-c]pyridine HCl

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:53885-53-3 SDS

53885-53-3Downstream Products

53885-53-3Relevant articles and documents

Method of making thieno-pyridine derivatives

-

, (2008/06/13)

The present invention provides a method of preparing thieno[3,2-c]pyridine derivatives of formula I: wherein R1 is selected from the group consisting of lower alkyl; lower alkylene phenyl; substituted lower alkylene phenyl wherein the phenyl is substituted from 1 to 3 times with lower alkyl, lower alkoxy, lower acyloxy, hydroxy, nitro and halo; lower alkylene naphthyl, lower alkylene thienyl; lower alkylene diphenyl; lower alkylene-hydroxy-phenyl; substituted lower alkylene-hydroxy-phenyl wherein the phenyl is substituted from 1 to 3 times with lower alkyl, lower alkoxy, lower acyloxy, hydroxy, nitro, and halo; lower alkylene-hydroxy-naphthyl; lower alkylene-hydroxy-thienyl; lower alkylene-hydroxy-diphenyl, and R2 is H or lower alkylene. The method comprises reacting a compound of a formula II: with a cyclic dioxy or cyclic dithio in the presence of catalyst.

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