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6946-10-7

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6946-10-7 Usage

General Description

1,3-Diacetoxyacetone is a chemical compound with the molecular formula C6H10O4. It is an organic compound that belongs to the class of ketones and is commonly used as a building block in organic synthesis. It is a clear, colorless liquid that is soluble in water and has a sweet, fruity odor. 1,3-Diacetoxyacetone is commonly used in the production of pharmaceuticals, agrochemicals, and other fine chemicals. It is also used as a reagent in chemical research and has applications in the manufacturing of flavor and fragrance compounds. The compound is considered to be relatively stable and non-reactive under normal conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 6946-10-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6946-10:
(6*6)+(5*9)+(4*4)+(3*6)+(2*1)+(1*0)=117
117 % 10 = 7
So 6946-10-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O5/c1-5(8)11-3-7(10)4-12-6(2)9/h3-4H2,1-2H3

6946-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Diacetoxyacetone

1.2 Other means of identification

Product number -
Other names (3-acetyloxy-2-oxopropyl) 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:6946-10-7 SDS

6946-10-7Relevant articles and documents

Prebiotic carbohydrate synthesis: Zinc-proline catalyzes direct aqueous aldol reactions of α-hydroxy aldehydes and ketones

Kofoed, Jacob,Reymond, Jean-Louis,Darbre, Tamis

, p. 1850 - 1855 (2007/10/03)

Zn-proline catalyzed aldolisation of glycoladehyde gave mainly tetroses whereas in the cross-aldolisation of glycoladehyde and rac-glyceraldehyde, pentoses accounted for 60% of the sugars formed with 20% of ribose. The Royal Society of Chemistry 2005.

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