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2,3-Nonanedione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57644-90-3

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57644-90-3 Usage

Synthesis Reference(s)

Tetrahedron Letters, 24, p. 2361, 1983 DOI: 10.1016/S0040-4039(00)81925-5

Check Digit Verification of cas no

The CAS Registry Mumber 57644-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,4 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57644-90:
(7*5)+(6*7)+(5*6)+(4*4)+(3*4)+(2*9)+(1*0)=153
153 % 10 = 3
So 57644-90-3 is a valid CAS Registry Number.

57644-90-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name nonane-2,3-dione

1.2 Other means of identification

Product number -
Other names 2,3-nonanedione

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:57644-90-3 SDS

57644-90-3Downstream Products

57644-90-3Relevant articles and documents

Cobalt(II)-Catalyzed Reaction of Aldehydes with Acetic Anhydride under an Oxygen Atmosphere: Scope and Mechanism

Bhatia, Beena,Punniyamurthy, T.,Iqbal, Javed

, p. 5518 - 5523 (2007/10/02)

The reaction of aldehydes with acetic anhydride in the presence of catalytic cobalt(II) chloride under an oxygen atmosphere at ambient temperature is dependent upon the reaction medium.Aliphatic aldehydes react in acetonitrile to give 1,2-diones whereas the aromatic aldehydes are acylated to yield the corresponding acylals.On the other hand, carboxylic acids are obtained from aliphatic and aromatic aldehydes by conducting the reaction in dichloroethane or benzene.Cobalt(II) chloride in acetonitrile catalyzes the conversion of aliphatic aldehydes to the correspondinganhydrides in the absence of acetic anhydride whereas aromatic aldehydes remain largely unaffected under these conditions.A preliminary mechanistic study in three different solvents (i.e. acetonitrile, dichloroethane, and DMF) has revealed that in acetonitrile and in the presence of acetic anhydride, aliphatic aldehydes behave differently than aromatic aldehydes.Some trapping experiments using methyl acrylate and stilbene have been conducted to demonstrate the occurence of an acyl cobalt and peroxyacyl cobalt intermediate during these reactions.

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