161891-31-2 Usage
Description
(E)-3-(4-bromophenyl)-3-chloro-prop-2-enal, also known as 4-Bromo-3-chlorocinnamaldehyde, is a chemical compound characterized by its molecular formula C9H6BrClO. This aldehyde features a bromophenyl group and a chloro group attached to a prop-2-enal chain, which contributes to its unique chemical properties and potential applications in various industries.
Uses
Used in Chemical Synthesis:
(E)-3-(4-bromophenyl)-3-chloro-prop-2-enal is utilized as a building block in the synthesis of other organic compounds, particularly those requiring the presence of a bromophenyl or chloro group. Its structural diversity makes it a valuable component in creating a wide range of chemical products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (E)-3-(4-bromophenyl)-3-chloro-prop-2-enal serves as a starting material for the production of fine chemicals and pharmaceutical intermediates. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Biological and Pharmacological Research:
(E)-3-(4-bromophenyl)-3-chloro-prop-2-enal has been studied for its potential biological and pharmacological properties. Researchers are interested in exploring its interactions with biological systems and its possible use in the development of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 161891-31-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,8,9 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 161891-31:
(8*1)+(7*6)+(6*1)+(5*8)+(4*9)+(3*1)+(2*3)+(1*1)=142
142 % 10 = 2
So 161891-31-2 is a valid CAS Registry Number.
161891-31-2Relevant articles and documents
Synthesis of novel β-aryl-β-(methylthio)acroleins via Vilsmeier-Haack protocol as potential 1,3-dielectrophilic three-carbon building blocks
Byre Gowda,Charanraj,Pradeepa Kumara,Ramesh,Thomas,Sadashiva,Junjappa
, p. 4475 - 4479 (2014/08/05)
A new general route for the synthesis of novel β-aryl-β- (methylthio)acroleins, a class of stable potential 1,3-dielectrophilic synthons, has been reported. The overall protocol involves treatment of either β-chloroacroleins or their precursor iminium salts (generated in situ from the corresponding active methylene ketones under Vilsmeier-Haack reaction conditions) with S,S-dimethyldithiocarbonates (DDC)/aqueous KOH in either a one-pot or two-step process. The dimethyldithiocarbonate (DDC)/30% aqueous KOH has been shown to be an excellent source of methylthiolate anion.
