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1072-89-5

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1072-89-5 Usage

General Description

4,5-Dimethyl-1,3-dihydro-2H-imidazol-2-one, also known as DMDO, is a chemical compound belonging to the class of organic compounds known as azolinones, which are heterocyclic compounds containing either an oxazoline, thiazoline, or an imidazoline moiety. It is a versatile synthetic reagent used widely in organic synthesis. The compound is known for its utility in the oxidation of primary and secondary alcohols to aldehydes and ketones, respectively. Additionally, DMDO can also be used for the epoxidation of alkenes. It is a solid white substance with a high melting point and low water solubility, used primarily in laboratory and industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 1072-89-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1072-89:
(6*1)+(5*0)+(4*7)+(3*2)+(2*8)+(1*9)=65
65 % 10 = 5
So 1072-89-5 is a valid CAS Registry Number.

1072-89-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-dimethyl-1,3-dihydroimidazol-2-one

1.2 Other means of identification

Product number -
Other names HMS1733G12

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:1072-89-5 SDS

1072-89-5Downstream Products

1072-89-5Relevant articles and documents

SYNTHESIS OF 4-METHYL-5-ALKYL-2-IMIDAZOLINONES

Zav'yalov, S. I.,Sitkareva, I. V.,Dorofeeva, O. V.,Rumyantseva, E. E.

, p. 1750 - 1752 (2007/10/02)

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Studies on acetylenic compounds. XXV. Ring closure. (5). New synthetic method of heterocyclic compounds from alpha-amino- and alpha-N-substituted amino- acetylenic compounds.

YURA

, p. 1087 - 1093 (2007/10/04)

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