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56323-20-7

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56323-20-7 Usage

General Description

1,1,4,4-tetramethylbutane-1,4-diyl diacetate is a chemical compound with the molecular formula C12H22O4. It is a diester obtained from the reaction of 1,1,4,4-tetramethylbutane-1,4-diol with acetic acid. 1,1,4,4-tetramethylbutane-1,4-diyl diacetate is commonly used as a solvent, plasticizer, or intermediate in the synthesis of various other chemicals. It has a clear, colorless appearance and is slightly soluble in water but highly soluble in organic solvents. 1,1,4,4-tetramethylbutane-1,4-diyl diacetate is used in industries such as chemical manufacturing, pharmaceuticals, and personal care products. It poses low toxicity and is considered to have minimal environmental impact.

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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