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Propanedioic acid, [2-(3-chlorophenyl)ethyl]-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119035-44-8

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119035-44-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119035-44-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,0,3 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 119035-44:
(8*1)+(7*1)+(6*9)+(5*0)+(4*3)+(3*5)+(2*4)+(1*4)=108
108 % 10 = 8
So 119035-44-8 is a valid CAS Registry Number.

119035-44-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-[2-(3-chlorophenyl)ethyl]propanedioate

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:119035-44-8 SDS

119035-44-8Downstream Products

119035-44-8Relevant academic research and scientific papers

Tf2O-Promoted Intramolecular Schmidt Reaction of the ω-Azido Carboxylic Acids

Wang, Xue-Juan,Su, Yan,Li, Rui,Gu, Peiming

, p. 5816 - 5824 (2018)

A designed Tf2O-promoted intramolecular Schmidt reaction of 2-substituted ω-azido carboxylic acids was demonstrated. Tf2O was used as an activation reagent for the carboxylic acid, and ω-azido anhydride was in situ generated, releasing a molecular TfOH, which acted as an acid promoter for the Schmidt process. A series of 2-substituted pyrrolidines was produced and acetylated for better purification. The strategy was also efficient for conversion of a 4-substituted ω-azido carboxylic acid to the tricyclic lactam.

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