59503-00-3 Usage
Description
(E)-1-(2-Bromovinyl)-2-chlorobenzene is a chemical compound characterized by a benzene ring with a vinyl group at position 1 and a chloro and bromo substituent at positions 2 and 2, respectively. It is a colorless or light yellow liquid with a molecular formula of C8H6BrCl.
Uses
Used in Pharmaceutical Synthesis:
(E)-1-(2-Bromovinyl)-2-chlorobenzene is used as a building block for the synthesis of pharmaceuticals, contributing to the development of new drugs and medications.
Used in Agrochemical Synthesis:
In the agrochemical industry, (E)-1-(2-Bromovinyl)-2-chlorobenzene is utilized as a key component in the creation of various agrochemicals, such as pesticides and fertilizers, to enhance agricultural productivity.
Used in Organic Synthesis Research and Development:
(E)-1-(2-Bromovinyl)-2-chlorobenzene serves as a reagent and intermediate in organic synthesis, playing a crucial role in the advancement of research and development in the field of organic chemistry.
Safety Precautions:
Check Digit Verification of cas no
The CAS Registry Mumber 59503-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,0 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59503-00:
(7*5)+(6*9)+(5*5)+(4*0)+(3*3)+(2*0)+(1*0)=123
123 % 10 = 3
So 59503-00-3 is a valid CAS Registry Number.
59503-00-3Relevant articles and documents
Ultrasonically Assisted Decarboxylative Bromination of α,β-Unsaturated Carboxylic Acids under Vilsmeier-Haack Conditions
Kumar, M. Satish,Rajanna,Venkanna,Venkateswarlu,Sudhakar Chary
, p. 642 - 646 (2016)
An efficient method for decarboxylative bromination of cinnamic acids (α,β-unsaturated carboxylic acids or 3-arylpropenoic acids) was achieved under relatively mild conditions using Vilsmeier-Haack reagent and KBr in acetonitrile media. Vilsmeier-Haack reagent is prepared by using 1:1 ratio of oxychloride (SOCl2 or POCl3) and DMF under chilled condition. Ultrasonically assisted reactions underwent smoothly with highly significant rate enhancements and afforded bromostyrenes as products in very good yields even though the reactions were too sluggish.
