22427-00-5 Usage
Functional groups
Ether, Alkene, Halogen
Ether
The compound contains an oxygen atom bonded to two carbon atoms (R-O-R').
Alkene
The compound has a carbon-carbon double bond (C=C).
Halogen
The compound contains a bromine atom (Br) attached to a carbon atom.
Structure
1-bromobut-3-en-2-yl methyl ether
The structure consists of a 1-bromobut-3-ene backbone with a methyl group (CH3) attached to the oxygen atom.
Reactivity
Nucleophilic substitution, Reduction
Reduction reactions can also occur, such as the reduction of the carbon-carbon double bond or the bromine atom.
Applications
Organic synthesis, Pharmaceutical industry, Research and development
Organic synthesis
Used as a reagent in various chemical reactions.
Pharmaceutical industry
Utilized in the production of certain drugs.
Research and development
Potential applications in the synthesis of new molecules and materials.
Solvent properties
Solvent or intermediate in the manufacturing of other organic compounds
The compound can act as a solvent for other organic compounds or serve as an intermediate in their synthesis.
Physical state
Liquid at room temperature
The compound is likely to be a liquid at room temperature, based on its molecular size and structure.
Hazards
Potential irritant, toxic, or corrosive
As with many organic compounds, 1-bromobut-3-en-2-yl methyl ether may pose hazards such as being an irritant, toxic, or corrosive. Proper handling and safety precautions should be taken when working with 1-bromobut-3-en-2-yl methyl ether.
Check Digit Verification of cas no
The CAS Registry Mumber 22427-00-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,2 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22427-00:
(7*2)+(6*2)+(5*4)+(4*2)+(3*7)+(2*0)+(1*0)=75
75 % 10 = 5
So 22427-00-5 is a valid CAS Registry Number.
22427-00-5Relevant academic research and scientific papers
Boron Trifluoride Promoted Reaction of Alkyl Hypohalites with Alkenes. A New Synthesis of Fluoro Halides
Heasley, Victor L.,Gipe, Robert K.,Martin, Jody L.,Wiese, Harry C.,Oakes, Melanie L.,Shellhamer, Dale F.
, p. 3195 - 3199 (2007/10/02)
The reactions of the following alkenes with alkyl hypohalites and boron trifluoride (BF3) were investigated: cyclohexene (3), 1-hexene (8), trans-1,2-dichloroethylene (15), methyl acrylate (18), methyl crotonate (25), methyl isocrotonate (29), butadiene (33), methyl vinyl ketone (42), and styrene (45).Reactions of these alkenes with methyl hypochlorite (1) and BF3 in dichloromethane give fluoro chloride adducts as well as methoxy chlorides with the percentage of fluoro chlorides varying from 75percent for 29 to 8percent for 45.Fluoro bromide adducts are obtained with methyl hypobromite (2).Reactions with the tert-butyl hypohalites and BF3 also give fluoride incorporation.The percentage of fluoride incorporation with 1 or 2 is significantly greater in carbon tetrachloride than in dichloromethane.
CARBON-CARBON BOND FORMATION UNDER MILD CONDITIONS VIA TANDEM CATIONIC AZA-COPE REARRANGEMENT-MANNICH REACTIONS. A CONVENIENT SYNTHESIS OF POLYSUBSTITUTED PYRROLIDINES.
Overman,Kakimoto,Okazaki,Meier G. Patrick
, p. 6622 - 6629 (2007/10/02)
The reaction of aldehydes (or ketones) with 2-alkoxy(or hydroxy)-3-alkenamines achieves a general and high-yielding synthesis of polysubstituted 3-acylpyrrolidines (eq 5-9). This tandem cationic aza-Cope rearrangement-Mannich cyclization reaction (eq 1) o
