2-[[4-(4-Cyclohexylcyclohexyl)butyl]amino]ethanethiol sulfate

Base Information

Chemical Name:2-[[4-(4-Cyclohexylcyclohexyl)butyl]amino]ethanethiol sulfate
CAS No.:21209-21-2
Molecular Formula:C18H35NO3S2
Molecular Weight:377.6054
Hs Code.:
Mol file:21209-21-2.mol

Synonyms:

Suppliers and Price of 2-[[4-(4-Cyclohexylcyclohexyl)butyl]amino]ethanethiol sulfate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 3 raw suppliers

Chemical Property of 2-[[4-(4-Cyclohexylcyclohexyl)butyl]amino]ethanethiol sulfate

Chemical Property:

Melting Point:223 - 224.5 °C (methanol)
Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：100.08000
Density:1.139g/cm³
LogP:6.14070

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-[[4-(4-Cyclohexylcyclohexyl)butyl]amino]ethanethiol sulfate

There total 3 articles about 2-[[4-(4-Cyclohexylcyclohexyl)butyl]amino]ethanethiol sulfate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 22565-56-6
4-<4-Cyclohexyl-cyclohexyl>-butanol

: 21209-21-2
Thiosulfuric acid S-[2-(4-bicyclohexyl-4-yl-butylamino)-ethyl] ester

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine; thionyl chloride

With pyridine; thionyl chloride;

Reference yield:

: 857831-00-6
4-<4-Cyclohexyl-cyclohexyl>-buttersaeure

: 21209-21-2
Thiosulfuric acid S-[2-(4-bicyclohexyl-4-yl-butylamino)-ethyl] ester

Guidance literature:: Multi-step reaction with 3 steps

1: lithium aluminium tetrahydride

2: pyridine; thionyl chloride

With pyridine; lithium aluminium tetrahydride; thionyl chloride;