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10437-96-4

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10437-96-4 Usage

Appearance

Yellow crystalline solid

Molecular weight

212.2 g/mol

Common uses

Building block for various pharmaceuticals and agrochemicals in organic synthesis

Notable properties

Strong electron-withdrawing character due to the presence of both a carbonyl and a nitrile group

Reactions

Useful for reactions such as Michael additions, condensations, and cyclizations

Reactivity

Versatile reactivity and functional group compatibility making it an important intermediate in the preparation of various complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 10437-96-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,3 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10437-96:
(7*1)+(6*0)+(5*4)+(4*3)+(3*7)+(2*9)+(1*6)=84
84 % 10 = 4
So 10437-96-4 is a valid CAS Registry Number.

10437-96-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-oxobutanoyl)indene-1,3-dione

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:10437-96-4 SDS

10437-96-4Downstream Products

10437-96-4Relevant articles and documents

Synthesis of 2-Acetoacetyl- and 2-Oxaloacetyl-1,3-indandiones and Related Compounds

Hamama, W. S.,Hammouda, M.,Afsah, E. M.

, p. 897 - 900 (2007/10/02)

Claisen condensation of 2-acetyl-1,3-indandione (1) with ethyl acetate afforded the 2-acetoacetyl-1,3-indandione (2) which upon treatment with benzylamine and paraformaldehyde in a molar ratio of (1:1:2) and (1:2:4) afforded the piperidinone and the diaza

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