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129340-04-1

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129340-04-1 Usage

Chemical Structure

Tetrahydroisoquinoline derivative containing a carbonitrile group and a thiol group

Potential Applications

Pharmaceutical and medicinal chemistry

Biological Activities

Possible enzyme inhibition or receptor binding

Utility

Building block in the synthesis of new drug candidates

Research Need

Further study and experimentation required to elucidate precise properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 129340-04-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,3,4 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 129340-04:
(8*1)+(7*2)+(6*9)+(5*3)+(4*4)+(3*0)+(2*0)+(1*4)=111
111 % 10 = 1
So 129340-04-1 is a valid CAS Registry Number.

129340-04-1SDS

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 1-(4-methylphenyl)-3-sulfanylidene-5,6,7,8-tetrahydro-2H-isoquinoline-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 3-Mercapto-1-p-tolyl-5,6,7,8-tetrahydro-isoquinoline-4-carbonitrile

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:129340-04-1 SDS

129340-04-1Relevant articles and documents

Studies on fused 2(1H)-pyridenethiones: New routes for the synthesis of fused 1H-pyrazolo[3,4-b]pyridines and fused thieno[2,3-b]pyridines

Al-Kaabi, Sharifa Soltan,Elgemeie, Galal Eldin Hamza

, p. 2241 - 2245 (2017/03/31)

A synthesis of fused 1H-pyrazolo[3,4-b]pyridines and fused thieno[2,3-b]pyridines utilizing fused 2(1H)-pyridinethiones as starting components is described. The structures of the products were assigned and confirmed on the basis of their elemental analysi

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