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2,5-Cyclohexadiene-1,4-dione, 2-hexyl-, also known as 2-Hexyl-2,5-cyclohexadiene-1,4-dione, is an organic compound with the molecular formula C12H18O2. It is a colorless to pale yellow liquid with a molecular weight of 194.27 g/mol. 2,5-Cyclohexadiene-1,4-dione, 2-hexyl- is characterized by a cyclohexadiene ring with a 1,4-dione functional group and a hexyl side chain attached to the 2-position. It is used as an intermediate in the synthesis of various chemicals and pharmaceuticals, particularly in the production of fragrances and flavorings. Due to its reactive nature, it is essential to handle 2,5-Cyclohexadiene-1,4-dione, 2-hexyl- with care, following proper safety protocols.

4197-73-3

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4197-73-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4197-73-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,9 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4197-73:
(6*4)+(5*1)+(4*9)+(3*7)+(2*7)+(1*3)=103
103 % 10 = 3
So 4197-73-3 is a valid CAS Registry Number.

4197-73-3SDS

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-hexylcyclohexa-2,5-diene-1,4-dione

1.2 Other means of identification

Product number -
Other names Hexyl-chinon

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:4197-73-3 SDS

4197-73-3Downstream Products

4197-73-3Relevant academic research and scientific papers

Synthesis of 2-substituted hydroquinone derivatives from 1,4-benzoquinone and allyl ethers

Kaurich, Kevin J.,Deck, Paul A.

, p. 2191 - 2196 (2018)

B-Alkylpinacolboranes, derived from rhodium-catalyzed hydroboration of allyl ethers with pinacolborane, react with 1,4-benzoquinone under acidic, oxidizing conditions, to afford, after subsequent hydrogenation, 2-substituted hydroquinones in isolated, pur

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