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33948-36-6

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33948-36-6 Usage

General Description

2-Iodo-2-cyclohexen-1-one is a chemical compound with the molecular formula C6H7IO. It is a yellow to brown liquid with a faint odor, and it is primarily used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. 2-Iodo-2-cyclohexen-1-one is known for its ability to undergo various chemical reactions, including nucleophilic substitution and addition reactions. It is also used as a reagent in organic synthesis and as a building block for the preparation of other complex molecules. Its unique structure and functional groups make it a valuable tool in the field of organic chemistry, making it an important compound for research and development in the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 33948-36-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,9,4 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 33948-36:
(7*3)+(6*3)+(5*9)+(4*4)+(3*8)+(2*3)+(1*6)=136
136 % 10 = 6
So 33948-36-6 is a valid CAS Registry Number.

33948-36-6SDS

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 2-iodocyclohex-2-enone

1.2 Other means of identification

Product number -
Other names 2-BENZYLSULFANYL-4,5-DIHYDROTHIAZOLE

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:33948-36-6 SDS

33948-36-6Relevant articles and documents

Synthesis of α-iodo-α,β-unsaturated ketones by the reaction of α- silyl-α,β-unsaturated ketones with ICl or ICIl-AlCl3

Alimardanov, Asaf,Negishi, Ei-ichi

, p. 3839 - 3842 (2007/10/03)

Treatment of α-silyl-α,β-unsaturated enones, readily preparable as regio- and stereodefined compounds in high yields, with either 2 equiv, of ICl or one equiv, each of ICl and AlCl3 provides the corresponding α-iodo- α,β-unsaturated enones in h

A facile conversion of epoxides to β-halohydrins with silica gel-supported lithium halides

Kotsuki, Hiyoshizo,Shimanouchi, Tomoyasu

, p. 1845 - 1848 (2007/10/03)

A variety of epoxides are efficiently converted to the corresponding β-halohydrins with lithium halides supported on silica gel in dry media.

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