10288-13-8 Usage
Description
1,2-Dibromo-3-methylbutane, with the molecular formula C5H10Br2, is a halogenated organic compound characterized by the presence of two bromine atoms attached to a butane molecule. This colorless liquid exhibits a strong, pungent odor and is highly flammable. Due to its hazardous nature to the environment and human health, it is classified as toxic if inhaled and can cause skin and eye irritation. Therefore, it requires careful handling, storage, and adherence to safety measures in laboratory or industrial settings.
Uses
Used in Organic Synthesis:
1,2-Dibromo-3-methylbutane serves as an alkylating agent, playing a crucial role in various organic synthesis processes and research. Its reactivity and structural properties make it a valuable intermediate in the production of different organic compounds.
Used in Research:
In the field of scientific research, 1,2-dibromo-3-methylbutane is utilized for studying the properties and reactions of halogenated hydrocarbons. It aids researchers in understanding the behavior of such compounds under various conditions, contributing to the advancement of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 10288-13-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,8 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10288-13:
(7*1)+(6*0)+(5*2)+(4*8)+(3*8)+(2*1)+(1*3)=78
78 % 10 = 8
So 10288-13-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H10Br2/c1-4(2)5(7)3-6/h4-5H,3H2,1-2H3
10288-13-8Relevant articles and documents
One-pot synthesis of substituted styrenes from vicinal dibromoalkanes and arylboronic acids
Tikhonov,Vasil'ev,Chirskaya,Struchkova,Merkulova,Zlotin
, p. 122 - 129 (2008/02/08)
Dehydrobromination of vicinal dibromoalkanes in systems comprising 1,2-dimethoxy-ethane, N-butyl-N′-methylimidazolium tetrafluoroborate (or tetrabutylammonium bromide), and a base with subsequent palladium-catalyzed cross-coupling of the thus formed bromoalkenes with arylboronic acids furnished substituted styrenes. Springer Science+Business Media, Inc. 2007.
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.
One-pot Conversions of Amines into Olefins via Non-isolated Pyridinium Intermediates
Katritzky, Alan R.,Lloyd, Jeremy M.
, p. 2347 - 2352 (2007/10/02)
Secondary alkyl primary amines are converted by the pyrylium salt (1) directly at 20 deg C into olefins via the corresponding secondary carbenium ions.Isomeric olefin mixtures are elucidated and result from carbenium ion rearrangements.
