1-(Bromomethyl)cyclohex-1-ene

≥95%

Reagent Code: #132362
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CAS Number 37677-17-1

science Other reagents with same CAS 37677-17-1

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Weight 175.05 g/mol
Formula C₇H₁₁Br
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MDL Number MFCD17015937
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as a reactive intermediate in organic synthesis, this compound serves as an alkylating agent due to the presence of the bromomethyl group adjacent to a double bond. It is commonly employed in the preparation of cyclohexene derivatives, including pharmaceuticals and agrochemicals, where functionalization of the ring system is required. The allylic bromide functionality allows for substitution reactions under mild conditions, making it useful in the formation of carbon-carbon and carbon-heteroatom bonds. It also finds use in the synthesis of polymers and specialty chemicals where a reactive handle is needed for further modification. Caution is required during handling due to its lachrymatory and corrosive properties.

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inventory 1g
10-20 days ฿23,280.00

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1-(Bromomethyl)cyclohex-1-ene
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Used primarily as a reactive intermediate in organic synthesis, this compound serves as an alkylating agent due to the presence of the bromomethyl group adjacent to a double bond. It is commonly employed in the preparation of cyclohexene derivatives, including pharmaceuticals and agrochemicals, where functionalization of the ring system is required. The allylic bromide functionality allows for substitution reactions under mild conditions, making it useful in the formation of carbon-carbon and carbon-hete

Used primarily as a reactive intermediate in organic synthesis, this compound serves as an alkylating agent due to the presence of the bromomethyl group adjacent to a double bond. It is commonly employed in the preparation of cyclohexene derivatives, including pharmaceuticals and agrochemicals, where functionalization of the ring system is required. The allylic bromide functionality allows for substitution reactions under mild conditions, making it useful in the formation of carbon-carbon and carbon-heteroatom bonds. It also finds use in the synthesis of polymers and specialty chemicals where a reactive handle is needed for further modification. Caution is required during handling due to its lachrymatory and corrosive properties.

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