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38493-62-8

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38493-62-8 Usage

General Description

(2-chlorophenyl)(2-methylphenyl)methanol, also known as 2,2-dimethyl-3-phenylpropan-1-ol, is a chemical compound with the molecular formula C14H14ClOH. It is classified as a secondary alcohol and is commonly used as a precursor in the synthesis of other organic compounds. It has a white solid appearance and a melting point of around 90-92°C. (2-chlorophenyl)(2-methylphenyl)methanol is mainly used in the production of pharmaceuticals, agrochemicals, and fragrances. It is important to handle this chemical with care as it may cause irritation to the skin, eyes, and respiratory system, and may be harmful if swallowed or inhaled in large quantities.

Check Digit Verification of cas no

The CAS Registry Mumber 38493-62-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,9 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38493-62:
(7*3)+(6*8)+(5*4)+(4*9)+(3*3)+(2*6)+(1*2)=148
148 % 10 = 8
So 38493-62-8 is a valid CAS Registry Number.

38493-62-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-chlorophenyl)-(2-methylphenyl)methanol

1.2 Other means of identification

Product number -
Other names 2-Chlor-2'-methyl-benzhydrol

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:38493-62-8 SDS

38493-62-8Relevant articles and documents

Highly Enantioselective Cobalt-Catalyzed Hydroboration of Diaryl Ketones

Liu, Wenbo,Guo, Jun,Xing, Shipei,Lu, Zhan

supporting information, p. 2532 - 2536 (2020/04/02)

A highly enantioselective cobalt-catalyzed hydroboration of diaryl ketones with pinacolborane was developed using chiral imidazole iminopyridine as a ligand to access chiral benzhydrols in good to excellent yields and ee. This protocol could be carried out in a gram scale under mild reaction conditions with good functional group tolerance. Chiral biologically active 3-substituted phthalide and (S)-neobenodine could be easily constructed through asymmetric hydroboration as a key step.

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