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63242-23-9

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63242-23-9 Usage

Description

[1,1'-Biphenyl]-4-methanol,4'-bromo-a-phenylis a chemical compound characterized by the molecular formula C19H15BrO. It is a derivative of biphenyl, which is a hydrocarbon composed of two benzene rings connected together. This particular compound is distinguished by the presence of a bromine atom on one of the benzene rings, along with a phenyl group and a hydroxyl (OH) group. It appears as a white to off-white solid. Although its specific properties and applications are not extensively documented, related chemicals have been utilized in the creation of pharmaceuticals, dyes, and various industrial products. Given its structural attributes, [1,1'-Biphenyl]-4-methanol,4'-bromo-a-phenylmay hold potential for use in organic synthesis and materials science.

Uses

Used in Pharmaceutical Industry:
[1,1'-Biphenyl]-4-methanol,4'-bromo-a-phenylis used as an intermediate compound for the synthesis of various pharmaceuticals due to its unique structural features and the presence of a bromine atom, which can be significant in the development of new drugs.
Used in Dye Industry:
In the dye industry, [1,1'-Biphenyl]-4-methanol,4'-bromo-a-phenylis used as a starting material for the production of specific dyes. The bromine atom and the phenyl group in its structure contribute to the color and stability of the resulting dyes.
Used in Materials Science:
[1,1'-Biphenyl]-4-methanol,4'-bromo-a-phenylmay be utilized in materials science for the development of novel materials with specific properties. Its structural characteristics could be exploited to create materials with tailored characteristics for various applications, such as in electronics or coatings.
Used in Organic Synthesis:
As an organic compound with a bromine atom and phenyl group, [1,1'-Biphenyl]-4-methanol,4'-bromo-a-phenylis used as a building block in organic synthesis. It can be employed to create a range of other organic compounds with diverse applications, from pharmaceuticals to specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 63242-23-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,2,4 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63242-23:
(7*6)+(6*3)+(5*2)+(4*4)+(3*2)+(2*2)+(1*3)=99
99 % 10 = 9
So 63242-23-9 is a valid CAS Registry Number.

63242-23-9SDS

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 [4-(4-bromophenyl)phenyl]-phenylmethanol

1.2 Other means of identification

Product number -
Other names (4'-bromo-biphenyl-4-yl)-phenyl-methanol

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:63242-23-9 SDS

63242-23-9Downstream Products

63242-23-9Relevant articles and documents

Selective metal-halogen exchange of 4,4′-dibromobiphenyl mediated by lithium tributylmagnesiate

Dolman, Sarah J.,Gosselin, Francis,O'Shea, Paul D.,Davies, Ian W.

, p. 5092 - 5098 (2006)

A selective metal-halogen exchange/electrophilic quench protocol on 4,4′-dibromobiphenyl 4 that proceeds under non-cryogenic conditions is reported. This method provides an economic alternative to traditional transition-metal catalyzed cross-coupling chemistry to prepare various biaryls 7a-g. This novel route to functionalized biaryls was used as the basis for the kg-scale preparation of a biphenyl ketone 1, a key intermediate in the synthesis of a potent cathepsin K inhibitor.

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