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10351-06-1 Usage

General Description

2,3,5,6-Tetrachloropyridine-4-thiol is a chemical compound with the formula C5HCl4NS. It is a yellow crystalline solid that is classified as an organochlorine compound. This molecule possesses a pyridine ring with four chlorine atoms and a sulfur atom attached. It is commonly used in chemical synthesis as a reagent and in organic reactions. 2,3,5,6-Tetrachloropyridine-4-thiol is also used as an intermediate in the production of agrochemicals and pharmaceuticals. Due to its toxic and hazardous nature, proper handling and storage of this chemical are essential to prevent harm to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 10351-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,5 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10351-06:
51 % 10 = 1
So 10351-06-1 is a valid CAS Registry Number.



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


1.1 GHS Product identifier

Product name 2,3,5,6-tetrachloro-1H-pyridine-4-thione

1.2 Other means of identification

Product number -
Other names 2,3,5,6-Tetrachloro-4-pyridinethiol

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:10351-06-1 SDS

10351-06-1Downstream Products

10351-06-1Relevant articles and documents


Ager et al.

, p. 1507 (1969)



Sipyagin, A. M.,Pal'tsun, S. V.,Pomytkin, I. A.,Aleinikov, N. N.

, p. 56 - 59 (2007/10/02)

The reaction on 2,3,5,6-tetrachloro-4-trifluoromethylthiopyridine with various nucleophilic reagents has been studied.It was shown that CF3S group is readily replaced under the action of O- and S-nucleophiles.Competition was detected between replacement of an α-chlorine atom on the pyridine ring and of the fluorine-containing group under the action of N-nucleophilic reagents.New derivatives of trichlorotrifluoromethylthiopyridine with nitrogen-containing substituents have been synthesized.

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