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24106-86-3

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24106-86-3 Usage

General Description

2-(2-fluorobenzyl)acetoacetic acid ethyl ester is a chemical compound which belongs to the category of acetoacetic acid esters. It is made up of a fluorobenzyl group attached to the acetoacetic acid through a carbon chain, and an ethyl ester group attached to the carboxyl group of the acetoacetic acid. 2-(2-FLUOROBENZYL)ACETOACETIC ACID ETHYL ESTER has potential applications in the pharmaceutical and chemical industries, and it may be used as a precursor in the synthesis of various organic compounds. Additionally, it possesses certain chemical properties which make it suitable for use as a reagent in organic chemistry reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 24106-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,1,0 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24106-86:
(7*2)+(6*4)+(5*1)+(4*0)+(3*6)+(2*8)+(1*6)=83
83 % 10 = 3
So 24106-86-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H15FO3/c1-3-17-13(16)11(9(2)15)8-10-6-4-5-7-12(10)14/h4-7,11H,3,8H2,1-2H3

24106-86-3SDS

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-[(2-fluorophenyl)methyl]-3-oxobutanoate

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:24106-86-3 SDS

24106-86-3Relevant articles and documents

Carbonic anhydrase inhibitors: Synthesis and inhibition studies against mammalian isoforms I-XV with a series of 2-(hydrazinocarbonyl)-3-substituted-phenyl-1H-indole-5-sulfonamides

Guezel, Oezlen,Innocenti, Alessio,Scozzafava, Andrea,Salman, Aydin,Parkkila, Seppo,Hilvo, Mika,Supuran, Claudiu T.

experimental part, p. 9113 - 9120 (2009/04/11)

A series of 2-(hydrazinocarbonyl)-3-substitutedphenyl-1H-indole-5-sulfonamides possessing various 2-, 3- or 4- substituted phenyl groups with methyl-, halogeno- and methoxy- functionalities, as well as the perfluorophenyl moiety have been synthesized and

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