56757-75-6

Basic information

• Product Name: decane-1,10-diyl dicarbonochloridate
• CAS NO: 56757-75-6
• Molecular Formula: C₁₂H₂₀Cl₂O₄
• Molecular Weight: 299.1908
• Mol File: 56757-75-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 353.7°C at 760 mmHg
• Flash Point: 126.8°C
• Density: 1.167g/cm³
• Vapor Pressure: 3.52E-05mmHg at 25°C
• Refractive Index: 1.465
• CAS DataBase Reference: decane-1,10-diyl dicarbonochloridate(CAS DataBase Reference)
• NIST Chemistry Reference: decane-1,10-diyl dicarbonochloridate(56757-75-6)
• EPA Substance Registry System: decane-1,10-diyl dicarbonochloridate(56757-75-6)

Safety Data

• Hazardous Substances Data: 56757-75-6(Hazardous Substances Data)

Upstream product

• 75-44-5 phosgene 
• 112-47-0 1,10-Decanediol 

Downstream Products

• 2162-98-3 1,10-dichlorodecane 

Relevant articles and documents

MULTIFUNCTIONAL AND BIFUNCTIONAL DITHIOCARBOXYLATE COMPOUNDS, MONOFUNCTIONAL ALKOXYCARBONYL DITHIOCARBAMATE COMPOUND, A METHOD FOR THE PREPARATION OF ALKOXYCARBONYL DITHIOCARBAMATE COMPOUNDS AS WELL AS A METHOD FOR THE PREPARATION OF MULTIBLOCK COPOLYMERS BY MEANS OF RADICAL POLYMERISATION

The present invention relates to a multifunctional dithiocarboxylate compound. The present invention furthermore relates to a bifunctional dithiocarboxylate compound. The present invention also relates to a monofunctional alkoxycarbonyl dithiocarbamate compound. The present invention further relates to a method for the synthesis of alkoxycarbonyl dithiocarbamate compounds. In addition, the present invention relates to a method for the preparation of one or more polymers by means of a radical polymerisation process, using a monofunctional, a bifunctional or a multifunctional dithiocarboxylate compound.

A safe and efficient procedure to prepare alkyl and alkoxyalkyl chlorides and dichlorides by catalytic decomposition of the corresponding alkyl and alkoxyalkyl chloroformates and bischloroformates with hexabutylguanidinium chloride

Small amounts of hexabutylguanidinium chloride (0.01 mol%) decomposes pure chloroformates or bischloroformates with different lengths of carbon chains by a semicontinuous process to diminish run-away risk, leading to chloride compounds with high yield and purity.