5398-65-2

Usage

Physical state

Colorless liquid

Odor

Pungent

Classification

Halogenated organic compound

Structure

Cyclopropane derivative with two bromine atoms and a vinyl group

Uses

Intermediate in the synthesis of various organic compounds, reagent in organic synthesis, building block for specialty chemicals

Safety

Handle with care, follow proper safety protocols due to halogenated nature

InChI:InChI=1/C5H6Br2/c1-2-4-3-5(4,6)7/h2,4H,1,3H2

Upstream product

• 75-25-2 Bromoform 
• 106-99-0 buta-1,3-diene 
• 74-95-3 1,1-dibromomethane 

Downstream Products

• 5365-17-3 2,2-dibromocyclopropane-1-carboxylic acid 
• 102393-49-7 cyclohexyl cis-2-vinylcyclopropyl ketone 
• 71647-64-8 benzyl cis-2-vinylcyclopropyl ketone 
• 71647-73-9 7-phenyl-1-trimethylsiloxy-1,4-cycloheptadiene 
• 71647-78-4 2-phenyl-4-cyclohepten-1-one 
• 98668-78-1 (3Z,6Z,9Z)-1-{2-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-1-trimethylsilanyl-cyclopropyl}-pentadeca-3,6,9-trien-1-ol 
• 98668-79-2 C₃₉H₅₉ClOSi₂ 
• 98668-77-0 C₂₄H₃₅BrOSi₂ 
• 10563-01-6 vinylallene 
• 542-92-7 cyclopenta-1,3-diene 
• 15136-01-3 cis-1-bromo-2-vinylcyclopropane 

Relevant academic research and scientific papers

Enantiomerically pure 2,2-dibromocyclopropanecarboxylic acids, simple chiral building blocks

Simple chiral building blocks 1-(R)- and 1-(S)-2,2- dibromocyclopropanecarboxylic acids and 2-(R)-bromo-1-(S')- cyclopropanecarboxylic acids and their 1-methyl analogues, have been obtained on a preparatively useful laboratory scale.

DISULFIDE BIOCONJUGATION

Compounds and methods are provided for one-step functionalization of disulfide bonds in proteins.

Thermodynamic control of diastereoselectivity in the formal nucleophilic substitution of bromocyclopropanes

(Figure Presented) A new, general, and chemoselective protocol for the formal nucleophilic substitution of 2-bromocyclopropylcarboxamides is described. A wide range of alcohols and phenols can be employed as pronucleophiles in this transformation, providi

Synthese von funktionalisierten bi(cyclopropylidenen)

In view of the synthesis of attractive triafulvalene precursors 9, a series of bi(cyclopropylidenes) 8 with vinyl(8a), alkoxycarbonyl (8c-f), hydroxymethyl (8h), as well as protected hydroxymethyl groups (8g, 8i) have been prepared by simple one-pot react

Arachidonic acid analogs

Analogs of arachidonic acid are provided having the structure STR1 wherein R is CH2 OH or CO2 H and m is 1 or 2. These compounds are useful as inhibitors of leukotriene and prostaglandin biosynthesis and as such are useful an antiall

6-(Substituted-cycloalkylcarboxamide) penicillanic acids

Penicillins of the formula SPC1 Or a pharmaceutically-acceptable, nontoxic salt thereof, Wherein R1 and R2 are the same or different and each is hydrogen, fluorine, chlorine or bromine; or when R2 is hydrogen, R1 can also be cyano, hydroxyl, azido, amino or nitro; or R1 and R2 are bonded to a ring carbon atom and constitute a single oxygen atom; R3 is hydrogen, methyl, chlorine, bromine, cyano, methoxy or carboxyl; and n is 2 to 7; Are useful for their antibacterial activity.