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2-Cyclohexen-1-one, 2,3-dihydroxy- is an organic compound with the molecular formula C6H8O3. It is a derivative of cyclohexenone, featuring two hydroxyl groups attached to the 2 and 3 positions of the cyclohexene ring. 2-Cyclohexen-1-one,2,3-dihydroxy- is known for its unique chemical structure, which contributes to its reactivity and potential applications in various fields, such as pharmaceuticals and chemical synthesis. Due to its cyclic structure and functional groups, it exhibits specific chemical properties that make it a subject of interest for researchers and chemists.

4337-36-4

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4337-36-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4337-36-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,3 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4337-36:
(6*4)+(5*3)+(4*3)+(3*7)+(2*3)+(1*6)=84
84 % 10 = 4
So 4337-36-4 is a valid CAS Registry Number.

4337-36-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dihydroxy-cyclohex-2-enone

1.2 Other means of identification

Product number -
Other names 2,3-Dihydroxy-cyclohex-2-enon

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:4337-36-4 SDS

4337-36-4Relevant academic research and scientific papers

Oxidation of α,β-unsaturated carbonyl groups with ruthenium (III)- chloride and peracetic acid: A new access to α-oxo-ene-diols

Beifuss, Uwe,Herde, Andreas

, p. 7691 - 7692 (1998)

A one pot oxidation of cyclic unsaturated carbonyl and carboxylic compounds with ruthenium (III)-chloride and peracetic acid to the corresponding α-oxo-ene-diols (aci-reductones) has been developed.

Acyloxylation of 1-methoxycyclohex-1-ene and other enol ethers with dimethyl peroxydicarbonate

Schank,Beck,Pistorius,Rapold

, p. 964 - 968 (2007/10/02)

Acyloxylation of different types of enol ethers (derived from aldehydes and ketones) by dimethyl peroxydicarbonate (DPDC) results in either addition to the double bond or in a formal replacement of an allylic hydrogen by a methoxycarbonyloxy group forming vicinal oxygenated hydrocarbons. 1,3-Oxygenated products via monoacyloxylation could not be observed. The results are compared with copper(I)-catalyzed acyloxylations of 1-methoxycyclohex-1-ene (1a) by means of tert-butyl peroxycarboxylates 2a, b.

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