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Phenol, 4-chloro-2-(diphenylmethyl)-, also known as 4-chloro-2-benzhydrylphenol or 4-chloro-2-(phenylphenylmethyl)phenol, is an organic compound with the chemical formula C19H15ClO. It is a derivative of phenol, featuring a chloro substituent at the 4-position and a diphenylmethyl group at the 2-position. Phenol, 4-chloro-2-(diphenylmethyl)- is characterized by its white crystalline appearance and is soluble in organic solvents. It is primarily used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its chemical structure, it exhibits various properties, such as antioxidant activity and potential applications in the development of new materials. However, it is important to note that Phenol, 4-chloro-2-(diphenylmethyl)- may have certain health and environmental risks, and appropriate safety measures should be taken during its handling and use.

737-25-7

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737-25-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 737-25-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 737-25:
(5*7)+(4*3)+(3*7)+(2*2)+(1*5)=77
77 % 10 = 7
So 737-25-7 is a valid CAS Registry Number.

737-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzhydryl-4-chlorophenol

1.2 Other means of identification

Product number -
Other names Phenol,4-chloro-2-(diphenylmethyl)

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:737-25-7 SDS

737-25-7Downstream Products

737-25-7Relevant academic research and scientific papers

Simple Method for sp2-sp3 and sp3-sp3 Carbon-Carbon Bond Activation in 2-Substituted 1,3-Diketones

Aoyama, Tadashi,Hayakawa, Mamiko,Kubota, Sho,Ogawa, Sumire,Nakajima, Erika,Mitsuyama, Emi,Iwabuchi, Taku,Kaneko, Haruki,Obara, Rina,Takido, Toshio,Kodomari, Mitsuo,Ouchi, Akihiko

, p. 2945 - 2956 (2015)

Simple and efficient methods were developed for sp2-sp3 and sp3-sp3 C-C bond-activation reactions of 2-substituted 1,3-diketones. 3-Substituted 3-bromopentane-2,4-diones were deacylated in the presence of an aromatic compound and a silica gel supported Bronsted acid containing sulfonic groups. The carbocation formed by cleavage of the sp3-sp3 C-C bond of the dione alkylated the aromatic compound.

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