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6342-57-0

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6342-57-0 Usage

General Description

1,1-dimethoxybutan-2-one is a chemical compound with the molecular formula C6H12O3. It is also known by the common name "diacetone dimethyl acetal" and is classified as a ketone. This colorless liquid is used as a solvent and as an intermediate in the production of various chemicals. It has a fruity odor and is volatile. It is typically synthesized through the reaction of acetone with methanol in the presence of an acid catalyst. 1,1-dimethoxybutan-2-one is flammable and should be handled with care in a well-ventilated area. It is also used as a flavor and fragrance ingredient in certain applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6342-57-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6342-57:
(6*6)+(5*3)+(4*4)+(3*2)+(2*5)+(1*7)=90
90 % 10 = 0
So 6342-57-0 is a valid CAS Registry Number.

6342-57-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dimethoxybutan-2-one

1.2 Other means of identification

Product number -
Other names 2-oxo-butyraldehyde dimethylacetal

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:6342-57-0 SDS

6342-57-0Relevant articles and documents

Halogenated Epoxides. 61. Reactions of Selected Chlorooxiranes with Sodium Methoxide: About the Question of Acetylenic and Allenic Epoxides as Intermediates

Griesbaum, Karl,Lie, Giu Oan,Keul, Helmut

, p. 679 - 682 (2007/10/02)

Reactions of sodium methoxide with five chlorooxiranes (1, 3, 11, 18, and 19) and with the corresponding isomeric chlorocarbonyl compounds have been examined.In two cases the chlorooxirane and the corresponding chlorocarbonyl compound afforded the same products, however, in different yields.In the other cases the chlorooxiranes and the corresponding chlorocarbonyl compounds gave different products.It is concluded that chlorocarbonyl compounds are not formed to a large extent as intermediates.In the reactions of two chlorooxiranes (18 and 19) with sodium methoxide, acetylenic and allenic epoxides may be invoked as transient intermediates.

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