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19094-75-8

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19094-75-8 Usage

Uses

2-(2-Chloro-6-methylphenoxy)acetic Acid could be useful as an anticonvulsant and analgesic.

Check Digit Verification of cas no

The CAS Registry Mumber 19094-75-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,9 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19094-75:
(7*1)+(6*9)+(5*0)+(4*9)+(3*4)+(2*7)+(1*5)=128
128 % 10 = 8
So 19094-75-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClO3/c1-6-3-2-4-7(10)9(6)13-5-8(11)12/h2-4H,5H2,1H3,(H,11,12)

19094-75-8SDS

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-Chloro-6-methylphenoxyacetic acid

1.2 Other means of identification

Product number -
Other names Acetic acid, (2-chloro-6-methylphenoxy)-

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:19094-75-8 SDS

19094-75-8Downstream Products

19094-75-8Relevant articles and documents

Increased intensity of tert-butoxyl radical emission in 4-chloro-2- methylphenoxyacetic acid (MCPA) synthesis

Jezierski, Adam,Zakrzewski, Jerzy,Moszczyski, Wiesaw

, p. 1229 - 1232 (2007/10/03)

The important herbicide, 2-methyl-4-chlorophenoxyacetic acid (MCPA) was synthesized by the chlorination of 2-methylphenoxyacetic acid with tert-butyl hypochlorite in the presence of methyl N,N-dimethylglycinate as a catalyst, giving a high yield and regioselectivity. The reaction was investigated using the spin-trapping technique in electron paramagnetic resonance measurement conditions, with nitrosodurene as a spin trap. Increased intensity emission of the tert-butoxyl radical (2.9 times in relation to the starting level) was observed after the catalyst had been introduced into the reaction mixture, indicating a free radical mechanism for the reaction.

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