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Ethanone, 1-(5-methyl-6-oxabicyclo[3.1.0]hex-1-yl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

145801-12-3

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145801-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145801-12-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,8,0 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 145801-12:
(8*1)+(7*4)+(6*5)+(5*8)+(4*0)+(3*1)+(2*1)+(1*2)=113
113 % 10 = 3
So 145801-12-3 is a valid CAS Registry Number.

145801-12-3SDS

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 1,2-epoxy-1-acetyl-2-methylcyclopentane

1.2 Other means of identification

Product number -
Other names 1-(5-Methyl-6-oxa-bicyclo[3.1.0]hex-1-yl)-ethanone

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:145801-12-3 SDS

145801-12-3Downstream Products

145801-12-3Relevant academic research and scientific papers

Aerobic Ru-catalyzed epoxidations in fluorous biphasic system using new fluorous benzimidazolic ligands

Ragagnin, Gianna,Knochel, Paul

, p. 951 - 954 (2007/10/03)

An efficient ruthenium catalyzed fluorous biphasic epoxidation of alkenes with oxygen in the presence of a pyridine-benzimidazole ligand bearing perfluorinated ponytails is described. Excellent yields and reaction rates were obtained and the fluorous phase could be recycled up to ten times without any loss of activity.

Rearrangement of acyloxyoxiranes: A revised structure for the oxidation product of 5α-androst-16-ene-3α,17-diol 3-benzoate 17-acetate

Subbaraju,Urbanczyk-Lipkowska,Newaz,Manhas,Bose

, p. 10087 - 10092 (2007/10/02)

During the oxidation of conjugated enones to α-acyloxyoxiranes by m-chloroperbenzoic acid, the preferred sequence is epoxidation followed by Baeyer-Villiger oxidation. Rearrangement of acyloxyoxiranes to α-acyloxyketones, in situ, was observed. The α-keto

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