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62932-90-5

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62932-90-5 Usage

Description

2-Chloro-3'-hydroxyacetophenone is a chemical compound with the molecular formula C8H7ClO2. It is an aromatic ketone that contains a chlorine atom and a hydroxyl group attached to a phenyl ring. 2-Chloro-3'-hydroxyacetophenone is known for its potential applications in various fields due to its unique structure and properties.

Uses

Used in Pharmaceutical Industry:
2-Chloro-3'-hydroxyacetophenone is used as a building block for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Chloro-3'-hydroxyacetophenone serves as an essential intermediate in the production of various agrochemicals. Its role in this sector is crucial for the development of effective pesticides and other agricultural products.
Used in Organic Chemistry Research:
2-Chloro-3'-hydroxyacetophenone is utilized as an intermediate in the production of other organic compounds. Its versatility in organic synthesis makes it a valuable tool for researchers working on the development of new chemical entities.
Used in Antimicrobial and Antiviral Applications:
2-Chloro-3'-hydroxyacetophenone has been studied for its potential biological activities, including antimicrobial and antiviral properties. Its ability to combat infections makes it a promising candidate for further research and development in the field of infectious diseases.
Overall, 2-Chloro-3'-hydroxyacetophenone is a versatile chemical compound with a wide range of applications in various industries, particularly in the synthesis of pharmaceuticals and agrochemicals, as well as in organic chemistry research and potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 62932-90-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,3 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62932-90:
(7*6)+(6*2)+(5*9)+(4*3)+(3*2)+(2*9)+(1*0)=135
135 % 10 = 5
So 62932-90-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H7ClO2/c9-5-8(11)6-2-1-3-7(10)4-6/h1-4,10H,5H2

62932-90-5SDS

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-chloro-1-(3-hydroxyphenyl)ethanone

1.2 Other means of identification

Product number -
Other names Ethanone,2-chloro-1-(3-hydroxyphenyl)

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:62932-90-5 SDS

62932-90-5Upstream product

62932-90-5Relevant articles and documents

Preparation method of L-phenylephrine hydrochloride

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Paragraph 0063-0065, (2020/10/04)

The invention relates to a preparation method of L-phenylephrine hydrochloride, and specifically discloses a preparation method of L-phenylephrine hydrochloride, which comprises the steps of chlorination reaction, chiral reduction reaction, amination salifying and recrystallization. The preparation method has the advantages of cheap and easily available raw materials, simple operation process, loweconomic cost, high product yield and the like, and the product quality meets the standard requirements of Chinese Pharmacopoeia and European Pharmacopoeia.

Mild and efficient α-chlorination of carbonyl compounds using ammonium chloride and oxone (2KHSO5·KHSO4· K2SO4)

Swamy, Peraka,Kumar, MacHarla Arun,Reddy, Marri Mahender,Narender, Nama

supporting information; experimental part, p. 432 - 434 (2012/06/01)

A simple protocol for the α-monochlorination of ketones and 1,3-dicarbonyl compounds utilizing NH4Cl as a source of chlorine and Oxone as an oxidant in methanol without catalyst is presented. The reaction proceeds at ambient temperature in yields ranging from moderate to excellent.

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