36229-64-8

Basic information

• Product Name: Oxirane, 2,3-dibutyl-, (2R,3S)-rel-
• CAS NO: 36229-64-8
• Molecular Formula: C10H20O
• Molecular Weight: 156.268
• Mol File: 36229-64-8.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: Oxirane, 2,3-dibutyl-, (2R,3S)-rel-(CAS DataBase Reference)
• NIST Chemistry Reference: Oxirane, 2,3-dibutyl-, (2R,3S)-rel-(36229-64-8)
• EPA Substance Registry System: Oxirane, 2,3-dibutyl-, (2R,3S)-rel-(36229-64-8)

Safety Data

• Hazardous Substances Data: 36229-64-8(Hazardous Substances Data)

Upstream product

• 7433-78-5 cis-5-decene 
• 1942-46-7 5-decyne 
• 19689-19-1 5-decene 
• 7433-56-9 (E)-5-decene 
• 111-66-0 oct-1-ene 

Downstream Products

• 820-29-1 decan-5-one 
• 7433-78-5 cis-5-decene 
• 7433-56-9 (E)-5-decene 
• 134895-34-4 6-(Toluene-4-sulfonyl)-decan-5-ol 
• 19689-19-1 5-decene 

Relevant articles and documents

Rhenium complex-catalyzed Meinwald rearrangement reactions of oxiranes

The Meinwald rearrangement reaction of oxiranes to the corresponding carbonyl compounds is efficiently catalyzed by the ReBr(CO)5 complex.

Formation of persulphate from sodium sulphite and molecular oxygen catalysed by H5PV2Mo10O40-aerobic epoxidation and hydrolysis

The H5PV2Mo10O40 polyoxometalate catalysed the electron transfer oxidation of sulphite to yield a sulphite radical, SO3- that upon addition of O2 yielded a peroxosulphate species efficient for the H5PV2Mo10O40 catalysed epoxidation of alkenes. The acidic polyoxometalate further catalysed hydrolysis of the epoxide to give vicinal diols in high yields. This journal is

PROCESS FOR MAKING AND USING HOF.RCN

The invention relates to a process for making HOF.RCN and using it to oxidise organic substrates in a quick and safe way. The process comprises passing diluted fluorine through a conduit and RCN in water through another conduit into a microreactor to form HOF.RCN and reacting this with an organic substrates.