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3,5-Dibromo-4-hydroxybenzyl alcohol is an organic compound with the chemical formula C7H6Br2O2. It is a white crystalline solid that is soluble in water and various organic solvents. 3,5-DIBROMO-4-HYDROXYBENZYL ALCOHOL is characterized by the presence of two bromine atoms at the 3rd and 5th positions of the benzene ring, a hydroxyl group at the 4th position, and a benzyl alcohol group attached to the benzene ring. It is primarily used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactive functional groups, it can undergo various chemical reactions, such as esterification, etherification, and substitution, making it a versatile building block in organic synthesis.

2316-62-3

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2316-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2316-62-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,1 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2316-62:
(6*2)+(5*3)+(4*1)+(3*6)+(2*6)+(1*2)=63
63 % 10 = 3
So 2316-62-3 is a valid CAS Registry Number.

2316-62-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dibromo-4-(hydroxymethyl)phenol

1.2 Other means of identification

Product number -
Other names Benzenemethanol,3,5-dibromo-4-hydroxy

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:2316-62-3 SDS

2316-62-3Relevant academic research and scientific papers

Synthesis of biaryl compounds through three-component assembly: Ambidentate effect of the tert-butyldimethylsilyl group for regioselective diels-alder and hiyama coupling reactions

Akai, Shuji,Ikawa, Takashi,Takayanagi, Sho-Ichi,Morikawa, Yuki,Mohri, Shinya,Tsubakiyama, Masaya,Egi, Masahiro,Wada, Yasufumi,Kita, Yasuyuki

supporting information; experimental part, p. 7673 - 7676 (2009/04/10)

Two for the price of one: A method has been developed for the regiocontrolled synthesis of multisubstituted biaryl derivatives. This protocol involves the use of the tert-butyldimethylsilyl (TBDMS) group to direct the regioselective Diels-Alder reaction of a 3-TBDMS-benzyne with a furan derivative and a subsequent Hiyama cross-coupling reaction of the TBDMS group with aryl iodides (see scheme).

Synthesis of some hydroxymethylbromophenols of marine origin

Sudalai, A.,Rao, G. S. Krishna

, p. 858 - 859 (2007/10/02)

The hydroxymethylbromophenols 5, 7 and 9, isolated from marine source have been prepared in good yield.The bromo derivatives 1 and 2 of vanillin are demethylated to 4 and 6 which on borohydride reduction furnish 5 and 7 respectively.The dibromo-p-cresol (3) is oxidised to the aldehyde 8 which on borohydride reduction affords 9.

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