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Acetic acid, [(3,5-dichloro-6-fluoro-2-pyridinyl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62270-89-7

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62270-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62270-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,7 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62270-89:
(7*6)+(6*2)+(5*2)+(4*7)+(3*0)+(2*8)+(1*9)=117
117 % 10 = 7
So 62270-89-7 is a valid CAS Registry Number.

62270-89-7SDS

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-(3,5-dichloro-6-fluoropyridin-2-yl)oxyacetic acid

1.2 Other means of identification

Product number -
Other names 3,5-dichloro-6-fluoro-2-pyridinyloxyacetate

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:62270-89-7 SDS

62270-89-7Downstream Products

62270-89-7Relevant academic research and scientific papers

6-Fluoro-3,5-dihalo-2-pyridyloxy compounds

-

, (2008/06/13)

Compounds are prepared which correspond to the formula STR1 wherein X represents chloro, bromo or iodo; R' represents hydrogen or methyl and R represents carboxy (--COOH), the alkyl esters thereof (--COOR6 wherein R6 represents alkyl

Method of preparing alkyl halopyridinyloxyalkanoates

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, (2008/06/13)

A novel method for the preparation of alkyl halopyridinyloxyalkanoate compounds is disclosed, which comprises reacting a halopyridine with an alkyl alpha-hydroxy alkanoate in the presence of an alkali metal carbonate promoter. The ester products prepared from this method are useful as herbicides.

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