CAS 17247-58-4
:(bromomethyl)cyclobutane
Description:
Bromomethylcyclobutane is an organic compound characterized by a cyclobutane ring with a bromomethyl group attached. Its molecular structure consists of a four-membered carbon ring, which contributes to its unique strain and reactivity. The presence of the bromomethyl group introduces a halogen, making the compound more reactive than cyclobutane itself. This reactivity is primarily due to the electrophilic nature of the bromine atom, which can participate in various substitution and addition reactions. Bromomethylcyclobutane is typically a colorless to pale yellow liquid at room temperature and has a relatively low boiling point, indicative of its small molecular size and the presence of non-polar bonds. The compound is used in organic synthesis, particularly in the preparation of more complex molecules through reactions such as nucleophilic substitution. Safety precautions should be taken when handling this compound, as brominated compounds can be hazardous and may pose environmental risks. Overall, bromomethylcyclobutane serves as an important intermediate in synthetic organic chemistry.
Formula:C5H9Br
InChI:InChI=1/C5H9Br/c6-4-5-2-1-3-5/h5H,1-4H2
InChI key:InChIKey=FLHFTXCMKFVKRP-UHFFFAOYSA-N
SMILES:C(Br)C1CCC1
Synonyms:- 1-(Bromomethyl)cyclobutane
- Bromocyclobutylmethane
- Cyclobutane, (bromomethyl)-
- Cyclobutylmethyl bromide
- (Bromomethyl)cyclobutane
- Bromomethyl)cyclobutane
- Bromomethyl cyclobutane
- (Bromomethyl)cyclobutene
- (Bromomethyl)codobutane
- (BROMOMETHYL)CYCLOBUTANE 99%
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Found 6 products.
(Bromomethyl)cyclobutane
CAS:(Bromomethyl)cyclobutaneFormula:C5H9BrPurity:98%Color and Shape:Colourless LiquidMolecular weight:149.02895(Bromomethyl)cyclobutane
CAS:Formula:C5H9BrPurity:>98.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:149.03(Bromomethyl)cyclobutane
CAS:Bromomethylcyclobutane is a synthetic compound that inhibits the CCR5 receptor, which is a co-receptor for HIV. It has been shown to have antiviral activity against HIV and hepatitis C virus (HCV) in vitro. Bromomethylcyclobutane also has anticancer activity, and its structure can be used as a lead for developing new drugs with cancer therapeutic potential. Bromomethylcyclobutane binds to the serine protease domain of the δ opioid receptors and inhibits protein synthesis by inhibiting uptake of amino acids into cells. It also prevents the formation of cellular proteins by binding to the hydroxyl group on lysine residues on DNA or RNA.Formula:C5H9BrPurity:Min. 95%Molecular weight:149.03 g/mol
