English
Building Block
17247-58-4
Clear colorless liquid
Boiling point: 123-124 °C(lit.)
Density: 1.326 g/mL at 25 °C(lit.)
Storage temp.: Inert atmosphere,2-8°C
Product Description
Product Category | Building Block |
CAS NO | 17247-58-4 |
Product Specifications | Clear colorless liquid Boiling point: 123-124 °C(lit.) Density: 1.326 g/mL at 25 °C(lit.) Storage temp.: Inert atmosphere,2-8°C |
17247-58-4 (BROMOMETHYL)CYCLOBUTANE.pdf
(Bromomethyl)cyclobutane is produced by EASTFINE , and we are in charge of overseas selling . Not just trading company .
China,America,Brazil,England,Russia,Poland,India,Pakistan,NewZealand,Korea,Australia,Dubai,Turkey,Indonesia,UAE.
Yes , you can have (Bromomethyl)cyclobutane sample for starting the business , but it is not free
Please contact our sales team for more details.
(Bromomethyl)cyclobutane is primarily used as an intermediate in organic synthesis. It can be involved in reactions such as:
· Nucleophilic substitution reactions to introduce various functional groups.
· Ring-opening reactions to generate new structural motifs in larger molecules.
· As a starting material in the synthesis of complex molecules, including pharmaceuticals, agrochemicals, and materials.
The structure consists of a cyclobutane ring (a four-membered carbon ring) with a bromomethyl group (-CH2Br) attached to one of the carbons in the ring. The bromine atom is typically attached to a methylene group (-CH2) connected to the cyclobutane ring, making it a halomethyl derivative.
(Bromomethyl)cyclobutane can be synthesized through various methods, such as:
· Electrophilic substitution using a brominating agent like NBS (N-Bromosuccinimide) or Br2 in the presence of a free radical initiator.
· Direct halogenation of cyclobutane with bromine in certain solvents.
· Radical or ionic mechanisms in specific reaction conditions.
· Bromomethyl groups are reactive and can potentially form harmful compounds under certain conditions, so caution should be taken.
· It may be toxic if ingested or inhaled, and it can irritate the skin or eyes.
· Proper lab safety protocols (e.g., gloves, goggles, fume hood) should be followed when handling this compound.
· It is reactive due to the presence of the bromomethyl group, which can participate in nucleophilic substitution reactions (e.g., SN1 or SN2 reactions).
· The cyclobutane ring introduces strain, which may make the compound more reactive under certain conditions.
Yes, (Bromomethyl)cyclobutane can undergo ring-opening reactions, especially under certain conditions that promote strain relief in the cyclobutane ring. This can lead to the formation of new carbon-carbon bonds and is often used to synthesize more complex molecules.
(Bromomethyl)cyclobutane is relatively stable under standard laboratory conditions, but it can decompose or react under certain conditions, particularly when exposed to heat, light, or strong reagents that promote the reactivity of the bromomethyl group.
Yes, (Bromomethyl)cyclobutane can be a useful building block in polymer chemistry, particularly in the synthesis of materials or copolymers that require functionalized monomers. The bromomethyl group can serve as a reactive site for polymerization or crosslinking.
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