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122274-70-8

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122274-70-8 Usage

Appearance

white to yellow solid

Appearance

white to yellow solid

Usage

used in production of polymers, coatings, pharmaceuticals, and agrochemicals

Usage

building block in the synthesis of pharmaceuticals and agrochemicals.

Hazardous

should be handled with care

Production

used in the production of polymers and coatings

Check Digit Verification of cas no

The CAS Registry Mumber 122274-70-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,2,7 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 122274-70:
(8*1)+(7*2)+(6*2)+(5*2)+(4*7)+(3*4)+(2*7)+(1*0)=98
98 % 10 = 8
So 122274-70-8 is a valid CAS Registry Number.

122274-70-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-3-(3-chlorophenyl)prop-2-enoic acid

1.2 Other means of identification

Product number -
Other names (Z)-2-chloro-3-(3-chlorophenyl)acrylic acid

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:122274-70-8 SDS

122274-70-8Upstream product

122274-70-8Relevant articles and documents

Ru-catalyzed highly chemo- and enantioselective hydrogenation of γ-halo-γ,δ-unsaturated-β-keto esters under neutral conditions

Ma, Xin,Li, Wanfang,Li, Xiaoming,Tao, Xiaoming,Fan, Weizheng,Xie, Xiaomin,Ayad, Tahar,Ratovelomanana-Vidal, Virginie,Zhang, Zhaoguo

supporting information; experimental part, p. 5352 - 5354 (2012/06/30)

Finely-tuned ruthenium-catalyzed highly chemoselective and enantioselective hydrogenation of γ-halo-γ,δ-unsaturated-β-keto esters at the carbonyl group was achieved under neutral reaction conditions (ee up to 97%). Both olefin and alkenyl halogen moieties, which are labile under hydrogenation conditions, remained untouched during the reaction.

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