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23107-52-0

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23107-52-0 Usage

General Description

2-(hydroxymethyl)cyclobutan-1-one, also known as cyclobutanone, is a cyclic ketone compound with the chemical formula C5H8O2. It is a colorless liquid with a slightly sweet and fruity odor. 2-(hydroxymethyl)cyclobutan-1-one is used in the synthesis of pharmaceuticals and agricultural chemicals. It can also be used as a solvent and as a building block in the production of other chemicals. Cyclobutanone is considered to be a valuable intermediate in organic synthesis due to its reactivity and versatile applications. Additionally, it is used in the manufacturing of fragrances and flavors for various consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 23107-52-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,1,0 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23107-52:
(7*2)+(6*3)+(5*1)+(4*0)+(3*7)+(2*5)+(1*2)=70
70 % 10 = 0
So 23107-52-0 is a valid CAS Registry Number.

23107-52-0SDS

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-(hydroxymethyl)cyclobutanone

1.2 Other means of identification

Product number -
Other names 2-Hydroxymethyl-cyclobutanon

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:23107-52-0 SDS

23107-52-0Relevant articles and documents

Reaction of dimethoxycarbene with strained cyclic carbonyl compounds

Venneri,Warkentin

, p. 1194 - 1203 (2007/10/03)

A cyclopropanone, a cyclopropenone, cyclobutanones, a cyclobutane-1,3-dione, and a cyclobutene-1,2-dione reacted with dimethoxycarbene to afford acetals of the next larger ring by formal insertion of the carbene into a C-C bond α to the carbonyl group. When either of two saturated α-ring carbons could be involved in the process, the ring expansion was selective, affording primarily the product of apparent insertion into the more substituted ring bond. With 2,3-dimethoxycyclobutene-1,2-dione, insertion occurred between the carbonyl groups and with β-propiolactone it occurred at the lactone bond. β-Propiolactam, however, reacted by insertion of the carbene into the N-H bond.

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