14205-58-4 Usage
Derivative of propane
The compound is derived from propane, which means it is structurally similar to propane but has additional functional groups attached to it.
Benzene sulfonyloxy group
A benzene ring connected to a sulfonyl group (-SO2), which is an integral part of the compound and influences its reactivity and properties.
Bromine atom
A halogen atom present in the compound, which imparts reactivity and can participate in various chemical reactions.
Two bromomethyl groups
Two methyl groups (-CH3) attached to bromine atoms, further increasing the compound's reactivity and allowing it to participate in numerous chemical reactions.
Organic synthesis reagent
The compound is commonly used as a reagent in organic synthesis reactions, aiding in the formation of carbon-carbon and carbon-oxygen bonds.
Flame retardant potential
Due to the presence of bromine atoms, the compound has potential use as a flame retardant, helping to slow down or prevent the spread of fire.
Polymer production
The compound can be used in the production of polymers, contributing to the formation and stabilization of polymer chains.
Reactive nature
1-benzenesulfonyloxy-3-bromo-2,2-bis-bromomethyl-propane is highly reactive, which makes it useful in organic synthesis but also requires careful handling.
Health hazards
The compound may pose potential health hazards, so it is essential to handle it with care and follow proper safety precautions to minimize risks.
Check Digit Verification of cas no
The CAS Registry Mumber 14205-58-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,0 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14205-58:
(7*1)+(6*4)+(5*2)+(4*0)+(3*5)+(2*5)+(1*8)=74
74 % 10 = 4
So 14205-58-4 is a valid CAS Registry Number.
14205-58-4Relevant academic research and scientific papers
Dyachenko,Protasova,Ioffe,Steinschneider,Nefedov
, p. 2055 - 2058 (1979)
The formation of methylenecyclobutane in the reaction of tetrahaloneopentanes and related compounds with zinc is shown to proceed via organozinc intermediates.
