(E)-N-[2-(2-cyclohexylethylsulfanyl)ethyl]dec-2-enamide

Base Information

Chemical Name:(E)-N-[2-(2-cyclohexylethylsulfanyl)ethyl]dec-2-enamide
CAS No.:137089-36-2
Molecular Formula:C₂₀H₃₇NOS
Molecular Weight:339.586
Hs Code.:
Nikkaji Number:J389.419C
Mol file:137089-36-2.mol

Synonyms:2-(2-decenoylamino)ethyl-2-(cyclohexylethyl)sulfide;2-DECES

Suppliers and Price of (E)-N-[2-(2-cyclohexylethylsulfanyl)ethyl]dec-2-enamide

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
Packaging
price

TRC
(E)-N-[2-[(2-Cyclohexylethyl)thio]ethyl]-2-decenamide
10mg
$ 1890.00

Total 2 raw suppliers

Chemical Property of (E)-N-[2-(2-cyclohexylethylsulfanyl)ethyl]dec-2-enamide

Chemical Property:

Vapor Pressure:2.93E-10mmHg at 25°C
Boiling Point:503.3°C at 760 mmHg
PKA:14.50±0.46(Predicted)
Flash Point:258.2°C
PSA：57.89000
Density:0.954g/cm³
LogP:6.56320
XLogP3:7.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:13
Exact Mass:339.25958598
Heavy Atom Count:23
Complexity:311

Purity/Quality:

95% ^*data from raw suppliers

(E)-N-[2-[(2-Cyclohexylethyl)thio]ethyl]-2-decenamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCC=CC(=O)NCCSCCC1CCCCC1
Isomeric SMILES:CCCCCCC/C=C/C(=O)NCCSCCC1CCCCC1
Uses (E)-N-[2-[(2-Cyclohexylethyl)thio]ethyl]-2-decenamide, can be used as an anti-ulcerogenic. It inhibits stress-induced ulcer and low toxicity, and can maintain the content of phospholipase A2 and prostaglandin E2 in ulcerated rats induced by water immersed restrained stress.

Technology Process of (E)-N-[2-(2-cyclohexylethylsulfanyl)ethyl]dec-2-enamide

There total 4 articles about (E)-N-[2-(2-cyclohexylethylsulfanyl)ethyl]dec-2-enamide 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:

: 110232-46-7
(E)-dec-2-enoyl chloride

: 137089-36-2
2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide

Guidance literature:: Multi-step reaction with 3 steps

1: 1N NaOH / H₂O; CH₂Cl₂ / 1 h / Ambient temperature; pH 8.0

2: Bu₃P, water / methanol / 1 h / Ambient temperature

3: 1N NaOH / methanol; H₂O / 1.5 h / Ambient temperature

With sodium hydroxide; tributylphosphine; water; In methanol; dichloromethane; water;
DOI:10.1248/cpb.39.1546

Reference yield:

: 334-49-6
trans-2-decenoic acid

: 137089-36-2
2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide

Guidance literature:: Multi-step reaction with 4 steps

1: SOCl₂ / 4 h / Heating

2: 1N NaOH / H₂O; CH₂Cl₂ / 1 h / Ambient temperature; pH 8.0

3: Bu₃P, water / methanol / 1 h / Ambient temperature

4: 1N NaOH / methanol; H₂O / 1.5 h / Ambient temperature

With sodium hydroxide; thionyl chloride; tributylphosphine; water; In methanol; dichloromethane; water;
DOI:10.1248/cpb.39.1546

Reference yield:

: 112614-18-3
bis<2-(E-2-decenoylamino)ethyl> disulfide

: 137089-36-2
2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide

Guidance literature:: Multi-step reaction with 2 steps

1: Bu₃P, water / methanol / 1 h / Ambient temperature

2: 1N NaOH / methanol; H₂O / 1.5 h / Ambient temperature

With sodium hydroxide; tributylphosphine; water; In methanol; water;
DOI:10.1248/cpb.39.1546