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823222-03-3

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823222-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 823222-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,3,2,2 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 823222-03:
(8*8)+(7*2)+(6*3)+(5*2)+(4*2)+(3*2)+(2*0)+(1*3)=123
123 % 10 = 3
So 823222-03-3 is a valid CAS Registry Number.

823222-03-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-5-(trifluoromethyl)pyridine-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-Pyridinecarboxylic acid,2-bromo-5-(trifluoromethyl)

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:823222-03-3 SDS

823222-03-3Downstream Products

823222-03-3Relevant articles and documents

Logistic flexibility in the preparation of isomeric halopyridinecarboxylic acids

Cottet, Fabrice,Schlosser, Manfred

, p. 11869 - 11874 (2007/10/03)

Although there are many conceivable ways to funtionalize, and specifically carboxylate, 2-chloro-4-(trifluoromethyl)pyridine optionally at all three vacant positions, it is more straightforward to prepare only the 2-chloro-4- (trifluoromethyl)pyridine-3-carboxylic acid (1) from this precursor and the other 6-chloro-4-(trifluoromethyl)pyridine-2- and -3-carboxylic acids (2 and 3) from a different one, viz. 5-bromo-2-chloro-4-(trifluoromethyl)pyridine. In the same manner, it proved more convenient to convert 5-chloro-2-(trifluoromethyl) pyridine in only two of the corresponding acids (6 and 7) and to make the third one (8) from 3-bromo-5-chloro-2-(trifluoromethyl)pyridine as an alternative starting material. All model substrates for functionalization were readily accessible from the correspondingly substituted chloroiodopyridine through heavy halogen displacement by in situ generated (trifluoromethyl)copper. Graphical Abstract

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