24325-95-9 Usage
Uses
Used in Organic Synthesis:
(E)-2-bromo-2-butenenitrile is used as a starting material for the production of various chemical intermediates, which are essential in the creation of a wide range of organic compounds. Its role in this application is to provide a foundation for further chemical reactions and the development of more complex molecules.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, (E)-2-bromo-2-butenenitrile is utilized as a building block for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of new drugs with potential therapeutic applications, contributing to the advancement of medical treatments.
Used in Agrochemical Synthesis:
(E)-2-bromo-2-butenenitrile also finds application in the agrochemical industry, where it is used as a starting material for the synthesis of compounds with agricultural applications. These may include the development of new pesticides, herbicides, or other chemicals that aid in crop protection and enhancement.
Used as a Reagent in Organic Chemistry:
(E)-2-bromo-2-butenenitrile serves as a reagent in the preparation of a wide range of compounds, including butadiene derivatives, esters, and other nitriles. Its reactivity and functional groups make it a valuable tool in the synthesis of various organic compounds.
Used as a Reagent in Organometallic Chemistry:
In addition to its use in organic chemistry, (E)-2-bromo-2-butenenitrile is also employed as a reagent in organometallic chemistry. It is particularly useful for the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in the synthesis of complex organic molecules.
Safety Precautions:
Due to the potential hazardous nature of (E)-2-bromo-2-butenenitrile, it is crucial to handle (E)-2-bromo-2-butenenitrile with care and store it according to safety guidelines. Proper safety measures should be taken to minimize risks associated with its use in research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 24325-95-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,2 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24325-95:
(7*2)+(6*4)+(5*3)+(4*2)+(3*5)+(2*9)+(1*5)=99
99 % 10 = 9
So 24325-95-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H4BrN/c1-2-4(5)3-6/h2H,1H3/b4-2+
24325-95-9Relevant academic research and scientific papers
Preparation of α-haloacrylate derivatives via dimethyl sulfoxide-mediated selective dehydrohalogenation
Li, Wei,Li, Jianchang,Wan, Zhao-Kui,Wu, Junjun,Massefski, Walter
, p. 4607 - 4610 (2008/03/13)
(Chemical Equation Presented) Dimethyl sulfoxide causes α/β-dihalopropanoate derivatives to undergo efficient, selective dehydrohalogenation to form α-haloacrylate analogues. A variety of α-halo Michael acceptors were prepared in dimethyl sulfoxide under mild, base-free conditions, including the preparation of α-bromoacrolein and α-chloro- and bromoacrylonitriles. Synthesis of these molecules has been reported in the literature to be difficult. Among all the existing dehydrohalogenation procedures, this protocol is the most facile, practical, and environmentally benign process.
Elimination reaction over solid supports under microwave irradiation: Synthesis of functionalized alkenes
Saoudi, Aicha,Hamelin, Jack,Benhaoua, Hadj
, p. 4035 - 4038 (2007/10/03)
Treatment of 1,2-dibromocompounds with KF supported on alumina, or bentonite/E13N under microwave irradiation leads to an elimination reaction which produces functionalized alkenes in fair yields.
