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56323-20-7

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56323-20-7 Usage

Type of compound

Diester

Formation

Obtained from the reaction of 1,1,4,4-tetramethylbutane-1,4-diol with acetic acid

Common uses

a. Solvent
b. Plasticizer
c. Intermediate in the synthesis of various other chemicals

Appearance

Clear, colorless

Solubility

a. Slightly soluble in water
b. Highly soluble in organic solvents

Industries

a. Chemical manufacturing
b. Pharmaceuticals
c. Personal care products

Toxicity

Low

Environmental impact

Minimal

Check Digit Verification of cas no

The CAS Registry Mumber 56323-20-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,2 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56323-20:
(7*5)+(6*6)+(5*3)+(4*2)+(3*3)+(2*2)+(1*0)=107
107 % 10 = 7
So 56323-20-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O4/c1-9(13)15-11(3,4)7-8-12(5,6)16-10(2)14/h7-8H2,1-6H3

56323-20-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-acetyloxy-2,5-dimethylhexan-2-yl) acetate

1.2 Other means of identification

Product number -
Other names EINECS 260-110-1

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:56323-20-7 SDS

56323-20-7Downstream Products

56323-20-7Relevant articles and documents

Hydroacetoxylation of olefins with acetic acid genetated in situ from vinyl acetate in the presence of ruthenium complexes

Khusnutdinov,Shchadneva,Khisamova,Dzhemilev

experimental part, p. 155 - 160 (2011/05/03)

Ruthenium complexes catalyze the decomposition of vinyl acetate releasing the acetic acid and its subsequent addition to linear and cyclic olefins.

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