31053-84-6 Usage
Chemical structure
1-bromo-4-methyl-1-cyclohexene is an organic compound with a cyclohexene ring and a bromine atom attached to the first carbon and a methyl group attached to the fourth carbon.
Physical state
It is a colorless liquid at room temperature.
Family
It belongs to the family of cycloalkenes, which are cyclic hydrocarbons with at least one carbon-carbon double bond.
Organic synthesis
It is commonly used in the synthesis of various organic compounds.
Reagent
It serves as a reagent in chemical reactions.
Pharmaceutical production
It is used in the production of various pharmaceuticals.
Agrochemical production
It is also used in the production of agrochemicals.
Synthesis potential
It is known for its potential as a precursor for the synthesis of other important organic compounds through chemical reactions such as addition and substitution reactions.
Flammability
It is considered a flammable liquid.
Inhalation and ingestion risks
It may be harmful if inhaled or ingested, so it should be handled with caution.
Safety precautions
Proper handling, storage, and disposal methods should be followed to minimize the risk of exposure and potential hazards associated with 1-bromo-4-methyl-1-cyclohexene.
Check Digit Verification of cas no
The CAS Registry Mumber 31053-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,0,5 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 31053-84:
(7*3)+(6*1)+(5*0)+(4*5)+(3*3)+(2*8)+(1*4)=76
76 % 10 = 6
So 31053-84-6 is a valid CAS Registry Number.
31053-84-6Relevant academic research and scientific papers
Halogenative Deoxygenation of Ketones; Vinyl Bromides and/or gem-Dibromides by Cleavage of 1,3-Benzodioxoles (Ketone Phenylene Acetals) with Boron Tribromide
Napolitano, Elio,Fiaschi, Rita,Mastrorilli, Ettore
, p. 122 - 125 (2007/10/02)
Representative ketones 1 have been converted in generally good yields to the respective 1,3-benzodioxoles 5 by trans-acetalization of ketone dimethyl acetals with 1,2-dihydroxybenzene, and cleaved with boron tribromide. 1,3-Benzodioxoles derived from α-unbranched aliphatic ketones gave in general a mixture of vinyl bromides and gem-dibromides; pure gem-dibromides could be selectively obtained in most of cases using a suitable reaction time. 1,3-Benzodioxoles derived from α-branched ketones gave complex mixtures and their cleavage appears to be of little synthetic signifance. 1,3-Benzodioxoles of aromatic ketones gave vinyl bromides only.Aliphatic cyclic gem-dibromides 3 were converted to the respective vinyl bromides 2 by phase-transfer-catalysed dehydrobromination.
