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Benzeneacetic acid, 2-(2-hydroxyethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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 academic research and scientific papers

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

Lithium 2-(2-lithiomethylphenyl)ethanolate from isochroman: Easy preparation of substituted benzoxepines and functionalised arenes

Almena, Juan,Foubelo, Francisco,Yus, Miguel

, p. 3365 - 3374 (2007/10/02)

The reaction of isochroman (1) with an excess of lithium powder and a catalytic amount of DTBB (2.5 mol %) in THF at 20°C yields the title intermediate, which by reaction with different electrophiles (H2O, D2O, CO2 and carbonyl compounds) at temperatures ranging between -78 and 20°C yields, after hydrolysis, the corresponding products 3. Diols 3h-m, derived from benzaldehyde or ketones, give upon treatment with 85% phosphoric acid the corresponding benzoxepines 5h-m. In the other cases, Friedel-Crafts products resulting from a rearrangement of the first carbenium ion formed, are obtained.

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)-

Synthesis of Aromatic Annulated ε-Lactones

Meise, Werner,Arth, Christoph

, p. 163 - 166 (2007/10/02)

The synthesis of three isomeric benzoxepinones 2, 7 and 8 by oxidation of the ω-diols 1 and 6 with silver carbonate on Celite is reported. Key Words: ε-Lactones / Oxidation of ω-diols with silver carbonate on Celite

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