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136863-22-4

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136863-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136863-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,8,6 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 136863-22:
(8*1)+(7*3)+(6*6)+(5*8)+(4*6)+(3*3)+(2*2)+(1*2)=144
144 % 10 = 4
So 136863-22-4 is a valid CAS Registry Number.

136863-22-4SDS

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-[2-(2-hydroxyethyl)phenyl]acetic acid

1.2 Other means of identification

Product number -
Other names 2-(2-hydroxyethyl)phenylacetic 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:136863-22-4 SDS

136863-22-4Relevant articles and documents

The aldol type reaction catalyzed by arylmalonate decarboxylase - A decarboxylase can catalyze an entirely different reaction, aldol reaction

Terao, Yosuke,Miyamoto, Kenji,Ohta, Hiromichi

, p. 420 - 421 (2007/10/03)

The catalytic promiscuity of AMDase was demonstrated using a well-designed substrate based on the consideration of the reaction mechanism. As the reaction catalyzed by AMDase is supposed to proceed via an enolate intermediate, we expected that the enzyme

Synthesis of Isomeric Methyl ε-Hydroxycarboxylates

Arth, Christoph,Clemens, Martina,Meise, Werner

, p. 259 - 264 (2007/10/02)

The synthesis of the three isomeric methyl ε-hydroxycarboxylates 3, 6 and 10a in good overall yields is described. - Key Words: Methyl ε-hydroxycarboxylates / Carboxylic acids, ε-hydroxy- / Phenylalkanoic acids, o-(hydroxyalkyl)-

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