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3-CHLORO-2-METHOXY-5-(TRIFLUOROMETHYL)PYRIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

175136-17-1

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175136-17-1 Usage

Chemical Properties

Pale yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 175136-17-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,1,3 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 175136-17:
(8*1)+(7*7)+(6*5)+(5*1)+(4*3)+(3*6)+(2*1)+(1*7)=131
131 % 10 = 1
So 175136-17-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H10FNO4/c15-12-4-1-10(2-5-12)9-20-14-6-3-11(8-17)7-13(14)16(18)19/h1-8H,9H2

175136-17-1SDS

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 3-Chloro-2-methoxy-5-(trifluoromethyl)pyridine

1.2 Other means of identification

Product number -
Other names 3-chloro-2-methoxy-5-(trifluoromethyl)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:175136-17-1 SDS

175136-17-1Relevant articles and documents

Alcoholysis of trifluoromethyl groups attached to the pyridine ring

Qian, Xuhong,Liu, Shuyou

, p. 9 - 12 (2007/10/03)

In dimethylformamide solution, trifluoroethoxylation and methoxylation of 5-chloro-3-trifluoromethylpyridine (2) yield 5-chloro-3-tris(trifluoroethoxyl)methyl pyridine (2a) and a dimethyl ketal of 3-chloronicotinic acid anhydride (2b) with fluorines as leaving groups, respectively. The corresponding reactions of 2,3-dichloro-5-trifluoromethylpyridine (3) only yield the 2-alkoxy-substituted products 3a and 3b with chloro as the leaving group and the 2-dimethylamino product 3c which was formed by the action of solvent dimethylformamide as a nucleophile. Differences in their reaction behaviour and possible mechanisms are also discussed.

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