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1607-31-4

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1607-31-4 Usage

Type of compound

Cyclic ester

Structure

Contains a five-membered ring with oxygen atoms (dioxolane)

Derivative

Acetic acid derivative (due to the acetyloxy group attached to the carbon atom in the ring)

Applications

a. Solvent in various industries
b. Production of pharmaceuticals
c. Stabilizer for chemical reactions
d. Potential use in polymer and adhesive industries

Toxicity

Low toxicity

Safety

Considered relatively safe for use in commercial and industrial settings

Check Digit Verification of cas no

The CAS Registry Mumber 1607-31-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1607-31:
(6*1)+(5*6)+(4*0)+(3*7)+(2*3)+(1*1)=64
64 % 10 = 4
So 1607-31-4 is a valid CAS Registry Number.

1607-31-4SDS

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 (2-oxo-1,3-dioxolan-4-yl)methyl acetate

1.2 Other means of identification

Product number -
Other names 1,3-Dioxolan-2-one,4-[(acetyloxy)methyl]

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:1607-31-4 SDS

1607-31-4Relevant articles and documents

Selective Synthesis of Carbonates from Glycerol, CO 2, and Alkyl Halides Using tert -Butyltetramethylguanidine

Mihara, Masatoshi,Moroga, Kaname,Iwasawa, Tetsuo,Nakai, Takeo,Ito, Takatoshi,Ohno, Toshinobu,Mizuno, Takumi

supporting information, p. 1759 - 1764 (2018/07/21)

Herein, we describe the guanidine-promoted synthesis of carbonates from glycerol, CO 2, and alkyl halides. Specifically, a linear tricarbonate (1,2,3-tri- O -butoxycarbonylglycerol), a dicarbonate [butyl (2-oxo-1,3-dioxolan-4-yl)methyl carbonate] containing a linear and a cyclic moiety, and a cyclic monocarbonate (4-hydroxymethyl-2-oxo-1,3-dioxolan) were selectively obtained in good yields, which were strongly affected by the steric bulkiness of the guanidine group substituents. The developed method exhibits the advantages of high efficiency and mild conditions, thus being a powerful tool for the synthesis of value-added products from industrial by-products.

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