English
Building Block
7051-34-5
Clear colorless to slightly colored Liquid
Melting point: 87-90 °C
Boiling point: 105-107 °C(lit.)
Density: 1.392 g/mL at 25 °C(lit.)
Storage temp.: Inert atmosphere,2-8°C
Product Description
| Product Category | Building Block |
| CAS NO | 7051-34-5 |
| Product Specifications | Clear colorless to slightly colored Liquid Melting point: 87-90 °C Boiling point: 105-107 °C(lit.) Density: 1.392 g/mL at 25 °C(lit.) Storage temp.: Inert atmosphere,2-8°C |
7051-34-5 (BROMOMETHYL)CYCLOPROPANE.pdf
(Bromomethyl)cyclopropane 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)cyclopropane sample for starting the business , but it is not free
Please contact our sales team for more details.
(Bromomethyl)cyclopropane is a chemical compound where a bromomethyl group (-CH2Br) is attached to a cyclopropane ring. Its molecular formula is C4H7Br, and it consists of a three-membered cyclopropane ring with a bromomethyl group attached to one of the carbons.
(Bromomethyl)cyclopropane is used primarily in organic synthesis. It can serve as an intermediate in the production of various chemicals, including other cyclic compounds. It may also be involved in reactions where the bromomethyl group is a leaving group, enabling the formation of new bonds or structures in further chemical synthesis.
One common method for synthesizing (Bromomethyl)cyclopropane is through electrophilic substitution, where a bromine atom reacts with cyclopropane under the presence of a brominating agent like Br2 or HBr. The reaction generally occurs in the presence of heat or a catalyst to promote the substitution of a hydrogen atom with a bromomethyl group.
· Molecular Formula: C4H7Br
· Appearance: It is typically a colorless liquid or solid (depending on the temperature).
· Boiling Point: It has a relatively low boiling point due to its simple structure.
· Solubility: It is generally soluble in organic solvents like ether, acetone, and chloroform, but insoluble in water.
The bromomethyl group in (Bromomethyl)cyclopropane is reactive and can undergo:
· Nucleophilic substitution reactions (such as substitution with nucleophiles like alcohols, amines, or thiols).
· Ring-opening reactions: The strained cyclopropane ring is susceptible to ring-opening reactions, which can lead to the formation of new organic compounds.
· Elimination reactions: Under certain conditions, the bromomethyl group can be eliminated, leading to the formation of other intermediates.
The bromomethyl group (-CH2Br) is an electrophilic substituent that can act as a leaving group in chemical reactions. It introduces reactivity to the molecule, making it useful in various organic syntheses, particularly in the formation of other functional groups or cyclic compounds.
(Bromomethyl)cyclopropane is relatively stable under standard conditions, but its cyclopropane ring can be reactive due to the inherent ring strain. Under certain conditions (like heat or the presence of nucleophiles), the molecule can undergo ring-opening reactions or other transformations.
As with most bromine-containing compounds, proper safety precautions should be followed, including:
· Using gloves and goggles to protect against skin and eye exposure.
· Ensuring good ventilation in areas where the compound is handled, as bromine can be toxic and irritating.
· Handling it in a fume hood when performing reactions, as volatile and potentially hazardous byproducts can form.
While (Bromomethyl)cyclopropane itself may not be a direct drug candidate, it can serve as an intermediate in the synthesis of bioactive molecules, particularly those that incorporate cyclopropane rings or bromomethyl groups, which can be reactive in medicinal chemistry for modifying or synthesizing new compounds.
· Nucleophilic substitution: Substitution of the bromine atom with various nucleophiles like alcohols (to form ethers), amines (to form amines), or thiols (to form sulfides).
· Ring-opening reactions: The strained cyclopropane ring can open to form linear or branched chain products depending on the reaction conditions.
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