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1-Propanone, 1-(3-propyloxiranyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6124-59-0

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6124-59-0 Usage

Physical state

Colorless liquid

Odor

Sweet

Use

Intermediate in the synthesis of other chemicals

Health effects

Irritant to skin, eyes, and respiratory system

Industrial applications

Production of pharmaceuticals, plastics, and agricultural chemicals

Potential applications

Organic synthesis, solvent in chemical reactions

Check Digit Verification of cas no

The CAS Registry Mumber 6124-59-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,2 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6124-59:
(6*6)+(5*1)+(4*2)+(3*4)+(2*5)+(1*9)=80
80 % 10 = 0
So 6124-59-0 is a valid CAS Registry Number.

6124-59-0SDS

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-(3-propyloxiran-2-yl)propan-1-one

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:6124-59-0 SDS

6124-59-0Upstream product

6124-59-0Downstream Products

6124-59-0Relevant academic research and scientific papers

A Novel Oxidation of Internal Alkynes with Hydrogen Peroxide Catalyzed by Peroxotungsten Compounds

Ishii, Yasutaka,Sakata, Yasuyuki

, p. 5545 - 5547 (1990)

Internal alkynes underwent a novel oxidation with aqueous hydrogen peroxide catalyzed by peroxotungsten compounds under two-phase conditions using chloroform as the solvent, giving α,β-epoxy ketones and α,β-unsaturated ketones as principal products.The epoxidation of α,β-unsaturated ketones by this catalyst-oxidant system appeared to involve the electrophilic attack of the peroxo species to the double bond.

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