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66742-56-1

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66742-56-1 Usage

General Description

4-[(3,4-DICHLOROBENZYL)OXY]BENZALDEHYDE is a chemical compound with the molecular formula C14H10Cl2O2. It is an aromatic aldehyde that contains benzene and aldehyde functional groups, as well as a dichlorobenzyl group. 4-[(3,4-DICHLOROBENZYL)OXY]BENZALDEHYDE is commonly used in organic synthesis and pharmaceutical research as a building block for the preparation of various organic compounds and pharmaceutical drugs. It has also shown potential as an antimicrobial and antifungal agent. Furthermore, its aromatic and aldehyde functions make it suitable for use in perfumery and fragrance applications. Overall, 4-[(3,4-DICHLOROBENZYL)OXY]BENZALDEHYDE is a versatile chemical with diverse potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 66742-56-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,7,4 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66742-56:
(7*6)+(6*6)+(5*7)+(4*4)+(3*2)+(2*5)+(1*6)=151
151 % 10 = 1
So 66742-56-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H10Cl2O2/c15-13-6-3-11(7-14(13)16)9-18-12-4-1-10(8-17)2-5-12/h1-8H,9H2

66742-56-1SDS

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 4-[(3,4-dichlorophenyl)methoxy]benzaldehyde

1.2 Other means of identification

Product number -
Other names -

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:66742-56-1 SDS

66742-56-1Relevant articles and documents

Selected michael additions to thiophene-containing analogues of chalcone

Roman, Gheorghe

, p. 751 - 760 (2015/11/24)

Using thiophene-containing analogues of chalcone as substrates, a series of Michael additions were investigated. Thia-Michael addition of 4-chlorothiophenol led to 1-(substituted aryl)-3-(4-chlorophenylmercapto)-1-(2-thienyl)-1-propanones, whereas catalyt

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