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Benzenemethanol, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-α-methyl-, also known as 3,5-di-tert-butyl-4-hydroxy-α-methylbenzyl alcohol or 3,5-di-tert-butyl-4-hydroxytoluene methanol, is an organic compound with the chemical formula C14H24O2. It is a derivative of benzyl alcohol, featuring a benzene ring with two tert-butyl groups at the 3 and 5 positions, a hydroxyl group at the 4 position, and a methyl group at the α-carbon. Benzenemethanol, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-a-methyl- is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure provides stability and reactivity, making it a valuable building block in organic synthesis.

14681-20-0

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14681-20-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14681-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,8 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14681-20:
(7*1)+(6*4)+(5*6)+(4*8)+(3*1)+(2*2)+(1*0)=100
100 % 10 = 0
So 14681-20-0 is a valid CAS Registry Number.

14681-20-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-Di-tert-butyl-4-(1-hydroxyethyl)phenol

1.2 Other means of identification

Product number -
Other names -

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:14681-20-0 SDS

14681-20-0Relevant academic research and scientific papers

UNUSUAL DISPROPORTIONATION ENCOUNTERED IN THE ALUMINA-CATALYZED DEHYDRATION OF 4-(α-HYDROXYETHYL)PHENOLS

Kamogawa, Hiroyoshi,Watanabe, Motoshi,Oka, Saichiro,Nanasawa, Masato

, p. 793 - 794 (2007/10/02)

Alumina-catalyzed dehydrations of 4-(α-hydroxyethyl)phenols provided unusual disproportionation products: 4-ethylphenols and 4-acetylphenols and their tautomers.

Process for preparing hindered alkenyl phenols

-

, (2008/06/13)

Hindered alkenyl phenols, all of which can be used as antioxidants, and some of which can be used as monomers, can be prepared by the dehydrohalogenation of the α-haloalkyl phenol.

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