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1020929-37-6

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1020929-37-6 Usage

Physical state

White crystalline solid This compound appears as a white, crystalline solid at room temperature.

Solubility

Soluble in organic solvents It can dissolve in organic solvents such as ethanol, acetone, and dichloromethane.

Synthesis use

Pharmaceutical and organic compounds 2-[(2-bromophenyl)methoxy]benzenemethanol is used as a starting material or intermediate in the synthesis of various pharmaceuticals and organic compounds.

Key intermediate

Biologically active molecules This compound serves as a key intermediate in the preparation of different biologically active molecules, which can have various therapeutic or chemical properties.

Bromine atom

Valuable reagent in organic chemistry reactions The presence of a bromine atom in its structure makes 2-[(2-bromophenyl)methoxy]benzenemethanol a valuable reagent for various organic chemistry reactions, such as electrophilic aromatic substitution and radical reactions.

Potential applications

Pharmaceutical and chemical industries Due to its versatile and valuable properties, 2-[(2-bromophenyl)methoxy]benzenemethanol has potential applications in both the pharmaceutical and chemical industries for the development of new drugs, agrochemicals, and other products.

Check Digit Verification of cas no

The CAS Registry Mumber 1020929-37-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,0,9,2 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1020929-37:
(9*1)+(8*0)+(7*2)+(6*0)+(5*9)+(4*2)+(3*9)+(2*3)+(1*7)=116
116 % 10 = 6
So 1020929-37-6 is a valid CAS Registry Number.

1020929-37-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(2-bromobenzyloxy)phenyl]methanol

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:1020929-37-6 SDS

1020929-37-6Downstream Products

1020929-37-6Relevant articles and documents

Palladium-catalyzed intramolecular C-O bond formation: An approach to the synthesis of chiral benzodioxocines

Neogi, Arpita,Majhi, Tirtha P.,Achari, Basudeb,Chattopadhyay, Partha

, p. 330 - 336 (2008/09/18)

Palladium-catalyzed intramolecular aryl etherification using bulky binaphthylphosphane or bis(diphenylphosphanyl)ferrocene ligands is shown to be a convenient method for the synthesis of eight-membered oxygen heterocycles. Application of this methodology to a sugar derivative led to the synthesis of chiral benzodioxocine. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

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