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63930-59-6

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63930-59-6 Usage

General Description

3-oxocyclobutyl acetate is a chemical compound with the molecular formula C6H8O3. It is a colorless liquid with a fruity odor, commonly used as a flavoring agent in the food industry. It is also used in the production of fragrances and perfumes. 3-oxocyclobutyl acetate is a derivative of cyclobutane and is classified as a cyclic ketone. It is soluble in water and has low toxicity. 3-oxocyclobutyl acetate is also used in the synthesis of other organic compounds and as a reagent in chemical reactions. Overall, it is a versatile compound with various applications in the fields of food, fragrance, and industrial chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 63930-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,9,3 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63930-59:
(7*6)+(6*3)+(5*9)+(4*3)+(3*0)+(2*5)+(1*9)=136
136 % 10 = 6
So 63930-59-6 is a valid CAS Registry Number.

63930-59-6SDS

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 (3-oxocyclobutyl) acetate

1.2 Other means of identification

Product number -
Other names 3-acetoxycyclobutanone

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:63930-59-6 SDS

63930-59-6Relevant articles and documents

Facile preparation of 3-acetoxycyclobutanone

Zajac, Matthew A.

, p. 4763 - 4764 (2008)

3-Acetoxycyclobutanone is a versatile intermediate to access cyclobutanes with a variety of substitution patterns. Established procedures require a two step process that includes multiple distillations. We report a one-pot procedure that renders this compound readily available. Additionally, it was determined that copper plays a key role in the reaction sequence.

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