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61623-62-9

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61623-62-9 Usage

Description

(4-bromophenyl)(diphenyl)methanol is a chemical compound with the molecular formula C19H15BrO. It is a white to off-white crystalline solid with a molecular weight of 329.23 g/mol. (4-bromophenyl)(diphenyl)methanol is known for its versatile chemical structure and reactivity, making it an important building block in the synthesis of various products.

Uses

Used in Pharmaceutical Industry:
(4-bromophenyl)(diphenyl)methanol is used as an intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into the molecular structures of various drugs. Its unique properties allow it to contribute to the development of new medications with potential therapeutic benefits.
Used in Agrochemical Industry:
In the agrochemical sector, (4-bromophenyl)(diphenyl)methanol serves as an intermediate in the production of agrochemicals, such as pesticides and herbicides. Its reactivity and structural features enable the creation of effective compounds designed to protect crops and enhance agricultural productivity.
Used in Organic Compounds Synthesis:
(4-bromophenyl)(diphenyl)methanol is utilized as a key intermediate in the synthesis of a wide range of organic compounds. Its versatility allows chemists to use it as a building block for creating complex organic molecules with diverse applications in various industries.
Used as a Reagent in Organic Synthesis and Chemical Research:
Due to its reactivity and structural characteristics, (4-bromophenyl)(diphenyl)methanol can be employed as a reagent in organic synthesis and chemical research. It aids in the development of new synthetic pathways and the exploration of novel chemical reactions, contributing to the advancement of scientific knowledge in these fields.
It is crucial to handle (4-bromophenyl)(diphenyl)methanol with care, as it may present potential hazards if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 61623-62-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,2 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61623-62:
(7*6)+(6*1)+(5*6)+(4*2)+(3*3)+(2*6)+(1*2)=109
109 % 10 = 9
So 61623-62-9 is a valid CAS Registry Number.

61623-62-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-bromophenyl)-diphenylmethanol

1.2 Other means of identification

Product number -
Other names 4-Brom-triphenylcarbinol

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:61623-62-9 SDS

61623-62-9Relevant articles and documents

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Mihailescu,Caragea

, ()

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Aspects of crystal engineering arising from packing behavior of functional mono para-substituted trityl compounds

Knepper, Ingo,Seichter, Wilhelm,Skobridis, Konstantinos,Theodorou, Vassiliki,Weber, Edwin

, p. 6355 - 6369 (2015/08/24)

Four trityl compounds differing both in the functional group (OH, OMe, NH2) at the specific trityl carbon and a para substituent, being bromine or phenyl at one of the phenyl groups, have been prepared and structurally studied by means of singl

Base-induced rearrangement of tritylamines to imines: discovery and investigation of the mechanism

Theodorou, Vassiliki,Skobridis, Konstantinos,Karkatsoulis, Aris

, p. 4284 - 4289 (2007/10/03)

An unexpected compound, the aniline derived benzophenone imine, was isolated when tritylamine was treated with n-BuLi and alkyl halides, during the formation of N-alkyl tritylamines, in the process of preparing primary amines. A nucleophilic attack of the nitrogen anion of tritylamide on the adjacent C-bonded phenyl, either substituted or not, involving a bridging anionic intermediate, is proposed for this base-induced tritylamine rearrangement to produce the corresponding imine. Electron-withdrawing groups in the aromatic ring, favoring the negative charge development, affect the relative migratory tendencies.

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