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24451-17-0

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24451-17-0 Usage

Chemical compound

2-Amino-2-oxo-acetic acid, N-[3,4-dimethylphenyl]-, ethyl ester
Commonly used in the pharmaceutical industry
Ethyl ester derivative of N-[3,4-dimethylphenyl]-2-amino-2-oxo-acetic acid
Known for its potential therapeutic properties
Used in the development of medicinal drugs
Potential applications in research and development
Valuable chemical with potential benefits in pharmaceutical and scientific endeavors

Check Digit Verification of cas no

The CAS Registry Mumber 24451-17-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,5 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 24451-17:
(7*2)+(6*4)+(5*4)+(4*5)+(3*1)+(2*1)+(1*7)=90
90 % 10 = 0
So 24451-17-0 is a valid CAS Registry Number.

24451-17-0SDS

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 ethyl 2-(3,4-dimethylanilino)-2-oxoacetate

1.2 Other means of identification

Product number -
Other names Ethyl (3,4-dimethylanilino)(oxo)acetate

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:24451-17-0 SDS

24451-17-0Downstream Products

24451-17-0Relevant articles and documents

2,2,2-Trifluoroethyl Chlorooxoacetate-Universal Reagent for One-Pot Parallel Synthesis of N1-Aryl-N2-alkyl-Substituted Oxamides

Bogolubsky, Andrey V.,Moroz, Yurii S.,Mykhailiuk, Pavel K.,Pipko, Sergey E.,Zhemera, Anton V.,Konovets, Anzhelika I.,Stepaniuk, Olena O.,Myronchuk, Inna S.,Dmytriv, Yurii V.,Doroschuk, Roman A.,Zaporozhets, Olga A.,Tolmachev, Andrey

, p. 615 - 622 (2015/10/28)

A one-pot parallel synthesis of N1-aryl-N2-alkyl-substituted oxamides with 2,2,2-trifluoroethyl chlorooxoacetate was developed. The synthesis of a library of 45 oxamides revealed higher efficiency of this reagent over the known ethyl chlorooxoacetate. The reagent was successfully used to prepare the known oxamide-containing HIV entry inhibitors.

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