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23147-57-1

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23147-57-1 Usage

General Description

3-Hydroxy-2-butanone dimer, more commonly known as acetoin dimer, is a chemical compound derived from acetoin, a colorless or pale yellow to green-yellow liquid with a pleasant, buttery odor. Acetoin, also known as 3-hydroxybutanone or acetyl methyl carbinol, is used in a variety of applications, including as a food flavoring and a fragrance. The acetoin dimer is synthesized by the dimerization of acetoin, and exhibits similar characteristics and uses to its monomer counterpart. As with most chemical compounds, it should be handled with care to prevent risks associated with exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 23147-57-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,1,4 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23147-57:
(7*2)+(6*3)+(5*1)+(4*4)+(3*7)+(2*5)+(1*7)=91
91 % 10 = 1
So 23147-57-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O4/c1-5-7(3,9)12-6(2)8(4,10)11-5/h5-6,9-10H,1-4H3

23147-57-1SDS

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 2,3,5,6-tetramethyl-1,4-dioxane-2,5-diol

1.2 Other means of identification

Product number -
Other names 2,3,4,5-TETRAHYDRO-7-METHOXY-1,4-BENZOTHIAZEPINE

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:23147-57-1 SDS

23147-57-1Downstream Products

23147-57-1Relevant articles and documents

UV-LIGHT- AND RADIATION-INITIATED ADDITION OF ACETALDEHYDE TO ALLYL ALKANOATES

Liska, Frantisek,Valenta, Miroslav,Fikar, Jiri,Jandova, Martina,Pesek, Miroslav,Trska, Petr

, p. 1287 - 1296 (2007/10/02)

UV-light- and γ-60Co-initiated addition of acetaldehyde to allyl formate (I) and allyl acetate (II) yielded the 1:1 adducts - 4-oxopentyl formate (III) and 4-oxopentyl acetate (IV), respectively, together with the 1:2 telomers - 7-formyloxy-4-formyloxymethyl-2-heptanone (V) and 7-acetoxy-4-acetoxymethyl-2-heptanone (VI).The initial radiation yields are: G(III) = 200.8, G(IV) = 211.3, G(V) = 39.5, G(VI) = 37.9.Base-catalyzed transesterification of oxopentyl alkanoates III and IV afforded 5-hydroxy-2-pentanone (XIV), the same reaction of dialkylalkanoates VI and VII gave 5-hydroxy-4-hydroxymethyl-2-heptanone (XV).

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