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1817-13-6

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1817-13-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1817-13-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,1 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1817-13:
(6*1)+(5*8)+(4*1)+(3*7)+(2*1)+(1*3)=76
76 % 10 = 6
So 1817-13-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H2Cl5N/c7-3-1-2-4(8)12-5(3)6(9,10)11/h1-2H

1817-13-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-DICHLORO-2-(TRICHLOROMETHYL)PYRIDINE

1.2 Other means of identification

Product number -
Other names 3,6-Dichloro-2-trichloromethylpyridine

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:1817-13-6 SDS

1817-13-6Relevant articles and documents

6-CHLORO-2-TRICHLOROMETHYL PYRIDINE PREPARATION METHOD

-

Page/Page column 5, (2010/04/23)

The present invention discloses a preparation method for 6-chloro-2-trichloromethyl pyridine, in which 2-methyl pyridine hydrochloride or 2-chloromethyl pyridine is used as an initiator and a considerably excess amount of chlorine gas reacts with 2-methyl pyridine hydrochloride or 2-chloromethyl pyridine at a high temperature to form purer 6-chloro-2-trichloromethyl pyridine. The present invention provides a highly selective, high-yield and improved environmental-ly protective method.

DESTRUCTIVE CHLORINATION OF 3,4,5-TRICHLORO-2-(TRICHLOROMETHYL)PYRIDINE

Emel'yanov, V. I.,Stul', B. Ya.,Korolev, B. M.

, p. 1168 - 1171 (2007/10/02)

The extensive destructive chlorination of 3,4,5-trichloro-2-(trichloromethyl)pyridine proceeds by both thermal (160-245 deg C) and photochemical pathways.Perchloropyridine, perchloropicoline, and carbon tetrachloride are formed.The chlorinated derivatives of pyridine are formed by the loss of the CCl3 group with its subsequent replacement by a chlorine atom.

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