2074-80-8 Usage
Uses
Used in Organic Synthesis:
2-Bromo-1-chloro-2-methylpropane is used as a reagent in organic synthesis for the production of various organic compounds. Its high reactivity allows it to participate in a wide range of chemical reactions, making it a versatile component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used as an Alkylating Agent:
In chemical reactions, 2-Bromo-1-chloro-2-methylpropane serves as an alkylating agent, facilitating the transfer of alkyl groups to other molecules. This property is useful in the synthesis of various organic compounds, including those with potential applications in the chemical, pharmaceutical, and materials science industries.
Used in Chemical Reactions:
2-Bromo-1-chloro-2-methylpropane is utilized in various chemical reactions due to its high reactivity. Its ability to participate in substitution, addition, and elimination reactions contributes to the formation of new compounds with desired properties. This makes it a valuable component in the development of novel materials and chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 2074-80-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,7 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2074-80:
(6*2)+(5*0)+(4*7)+(3*4)+(2*8)+(1*0)=68
68 % 10 = 8
So 2074-80-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H8BrCl/c1-4(2,5)3-6/h3H2,1-2H3
2074-80-8Relevant academic research and scientific papers
Bromochlorination of Alkenes with Dichlorobromate (1-) ion. IV. Regiochemistry of Bromochlorinations of Alkenes with Molecular Bromine Chloride and Dichlorobromate (1-) Ion
Negoro, Takeshi,Ikeda, Yoshitsugu
, p. 2547 - 2552 (2007/10/02)
The regioselectivity of the addition of molecular bromine chloride to alkenes is dependent on both the steric and electronic effects of the alkyl substituent.In contrast, the regioselectivity of the addition of dichlorobromate (1-) ion to alkenes is controlled mainly by the steric effect of the substituent.
