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37612-59-2

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37612-59-2 Usage

General Description

1-(3-chloro-4-ethoxyphenyl)ethanone, also known as ethyl 3-chloro-4-ethoxybenzoylacetate, is a chemical compound with the molecular formula C10H11ClO3. It is a yellow liquid that is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 1-(3-chloro-4-ethoxyphenyl)ethanone has a variety of industrial applications, including its use as a building block in the production of other organic compounds. It is also used in the synthesis of chiral catalysts and pharmaceutical products. Additionally, it is known to have antimicrobial and anti-infective properties.

Check Digit Verification of cas no

The CAS Registry Mumber 37612-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,1 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 37612-59:
(7*3)+(6*7)+(5*6)+(4*1)+(3*2)+(2*5)+(1*9)=122
122 % 10 = 2
So 37612-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClO2/c1-3-13-10-5-4-8(7(2)12)6-9(10)11/h4-6H,3H2,1-2H3

37612-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-Chloro-4-ethoxyphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 3-Chlor-4-ethoxyacetophenon

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:37612-59-2 SDS

37612-59-2Relevant articles and documents

Room temperature C(sp2)-H oxidative chlorination: Via photoredox catalysis

Zhang, Lei,Hu, Xile

, p. 7009 - 7013 (2017/10/05)

Photoredox catalysis has been developed to achieve oxidative C-H chlorination of aromatic compounds using NaCl as the chlorine source and Na2S2O8 as the oxidant. The reactions occur at room temperature and exhibit exclusive selectivity for C(sp2)-H bonds over C(sp3)-H bonds. The method has been used for the chlorination of a diverse set of substrates, including the expedited synthesis of key intermediates to bioactive compounds and a drug.

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