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111461-02-0

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111461-02-0 Usage

Molecular Weight

159.17 g/mol

Structure

A propanone molecule linked to a 5-hydroxy-3-methyl-4-isoxazolyl group

Usage

Commonly used in pharmaceutical research and drug development

Potential Biological Activities

Has potential medicinal properties and has been investigated for the treatment of various diseases and conditions

Safety and Efficacy

Further research needed to fully understand its therapeutic potential and safety profile.

Check Digit Verification of cas no

The CAS Registry Mumber 111461-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,4,6 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 111461-02:
(8*1)+(7*1)+(6*1)+(5*4)+(4*6)+(3*1)+(2*0)+(1*2)=70
70 % 10 = 0
So 111461-02-0 is a valid CAS Registry Number.

111461-02-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(5-Hydroxy-3-methyl-1,2-oxazol-4-yl)-2-methyl-1-propanone

1.2 Other means of identification

Product number -
Other names -

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:111461-02-0 SDS

111461-02-0Downstream Products

111461-02-0Relevant articles and documents

An Efficient Synthesis of 4-Acyl-5-hydroxy-3-methylisoxazoles through an Acyl-Transfer Reaction

Sato, Kazuo,Ueda, Takashi,Sugai, Soji

, p. 3153 - 3158 (2007/10/02)

Acylation of 3-methyl-3-isoxazolin-5-one (2a) with acyl chlorides was investigated. 2-Acyl-3-methyl-3-isoxazolin-5-ones 5 and 5-acyloxy-3-methylisoxazoles 6, which were prepared from 2a and acyl halides, underwent acyl-transfer reaction in the presence of

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