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2,3-Oxiranediethanol (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124353-41-9

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124353-41-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124353-41-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,3,5 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 124353-41:
(8*1)+(7*2)+(6*4)+(5*3)+(4*5)+(3*3)+(2*4)+(1*1)=99
99 % 10 = 9
So 124353-41-9 is a valid CAS Registry Number.

124353-41-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[3-(2-hydroxyethyl)oxiran-2-yl]ethanol

1.2 Other means of identification

Product number -
Other names 2,3-Oxiranediethanol (9CI)

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:124353-41-9 SDS

124353-41-9Upstream product

124353-41-9Downstream Products

124353-41-9Relevant academic research and scientific papers

Synthesis of (tetrahydrofiiranyl)tetrahydrofurans via radical cyclization of bis(-alkoxyacrylates)

Lee, Eun,Song, Ho Young,Kirn, Hee Jo

, p. 3395 - 3396 (1999)

Radical cyclizations of bis(-alkoxyacrylates) obtained from. (3R, 4R)- and mes0-l, 6-dibromohexane-3, 4-diol proceed to form a C2-symmetric and a nieso (tetrahydrofuranyl)tetrahydrofuran derivative. The Royal Society of Chemistry 1999.

Process for preparing aldehydes from oxirane compounds

-

, (2008/06/13)

Aldehydes are prepared by reacting an oxirane compound with hydrogen peroxide in the presence of a boron compound.

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