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2-Hexylbenzene-1,4-diol, also known as 4-(1-Hexyl)benzene-1,2-diol or 4-Hexylresorcinol, is an organic compound with the chemical formula C12H18O2. It is a colorless to pale yellow liquid with a molecular weight of 194.27 g/mol. 2-hexylbenzene-1,4-diol is characterized by a benzene ring with two hydroxyl groups at the 1 and 4 positions and a hexyl chain attached to the 4 position. It is used in various applications, including as a chemical intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its hydroxyl groups, 2-hexylbenzene-1,4-diol can participate in a range of chemical reactions, such as esterification, etherification, and condensation, making it a versatile building block in organic synthesis.

4197-72-2

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4197-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4197-72-2 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 4197-72:
(6*4)+(5*1)+(4*9)+(3*7)+(2*7)+(1*2)=102
102 % 10 = 2
So 4197-72-2 is a valid CAS Registry Number.

4197-72-2SDS

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-hexylbenzene-1,4-diol

1.2 Other means of identification

Product number -
Other names 2-hexyl-hydroquinone

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:4197-72-2 SDS

4197-72-2Relevant 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 (2018/03/28)

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

FUNCTIONALIZED PRIMARY ALKYLTRIFLUOROBORATE SALTS AND METHOD FOR MAKING THE SAME

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Paragraph 0100-0102, (2017/03/21)

The invention provides methods for preparing boronic acids, for example, primary alkyl or alkenyl boronic acids, and alkali metal alkyl trifluoro borate salts, as described herein, wherein the primary alkyl boronic acids and the potassium alkyl trifluoroborate salts can contain one or more unprotected functional groups.

Reductive alkylation of p-benzoquinone using mixed organoboranes

Zillman, David J.,Hincapié, Gloria C.,Reza Savari,Mizori, Farhad G.,Cole, Thomas E.

supporting information; experimental part, p. 3033 - 3036 (2010/08/05)

Mixed organoboranes based on diphenyl- or dimethylalkylboranes transfer the alkyl group in the reductive alkylation of p-benzoquinone to form the alkylhydroquinones in very high yields. The auxiliary groups do not transfer or have a low migratory aptitude. Primary and secondary alkyl groups are transferred with retention of regio- and stereochemistry to the hydroquinone. O-Alkylation is the major product with tertiary and secondary groups with steric bulk in proximity to the site of attachment. The presence of metal salts, such as magnesium, results in reduction to the unsubstituted hydroquinone. This reaction makes the first practical route to alkylhydroquinones via organoboranes.

METHODS FOR SYNTHESIZING ALKYLATED AND ALKENYLATED QUINONE DERIVATIVES

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Page/Page column 17-18, (2008/06/13)

The present invention relates to methods for preparing quinone derivatives comprising reacting quinones with organoborane reagents to produce alkylated and alkenylated quinone derivatives. In one embodiment, the present invention provides processes compri

A Convenient Synthesis of 2-Alkylated 1,4-Benzenediols

Ozaki, Yutaka,Hosoya, Ayako,Okamura, Kyouko,Kim, Sang-Won

, p. 365 - 366 (2007/10/03)

Reaction of 1,4-cyclohexanedione with a variety of aldehydes in the presence of metal halides generated the 2-alkylated 1,4-benzenediols in good yields without any aromatic by-products.

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