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Benzenepropanoic acid, a-diazo-b-hydroxy-3-(trifluoromethyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

442157-13-3

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442157-13-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 442157-13-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,2,1,5 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 442157-13:
(8*4)+(7*4)+(6*2)+(5*1)+(4*5)+(3*7)+(2*1)+(1*3)=123
123 % 10 = 3
So 442157-13-3 is a valid CAS Registry Number.

442157-13-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-diazo-3-hydroxy-3-(3-(trifluoromethyl)phenyl)propanoate

1.2 Other means of identification

Product number -
Other names -

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:442157-13-3 SDS

442157-13-3Relevant academic research and scientific papers

DBU-catalyzed condensation of acyldiazomethanes to aldehydes in water and a new approach to ethyl β-hydroxy α-arylacrylates

Xiao, Fengping,Liu, Yu,Wang, Jianbo

, p. 1147 - 1149 (2007/10/03)

DBU-catalyzed condensation of ethyl diazoacetate (EDA) with aldehydes in pure water afforded corresponding β-hydroxy α-diazo carbonyl compounds. The β-hydroxy group of the products was further converted into β-siloxy group. The Rh(II)-catalyzed reaction of the β-aryl β-siloxy α-diazo carbonyl compounds gave 1,2-aryl shift products predominantly. The three-step transformation constitutes an efficient synthesis of ethyl β-hydroxy α-arylacrylates.

DBU-promoted condensation of acyldiazomethanes to aldehydes and imines under catalytic conditions

Jiang, Nan,Wang, Jianbo

, p. 1285 - 1287 (2007/10/03)

The condensation of acyldiazomethanes to aldehydes and imines can be promoted with catalytic amount of DBU. The condensation gives β-hydroxy α-diazo carbonyl compounds or β-amino α-diazo carbonyl compounds in high yields.

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