6-(Methylsulfanyl)hexan-1-amine

Base Information

Chemical Name:6-(Methylsulfanyl)hexan-1-amine
CAS No.:62580-22-7
Molecular Formula:C7H17NS
Molecular Weight:147.28200
Hs Code.:
European Community (EC) Number:851-861-1
ChEMBL ID:CHEMBL3247585
DSSTox Substance ID:DTXSID20553361
Wikidata:Q82433922

Synonyms:6-(methylsulfanyl)hexan-1-amine;62580-22-7;6-methylsulfanylhexan-1-amine;7-thiaoctylamine;6-(Methylthio)hexan-1-amine;CHEMBL3247585;SCHEMBL11160081;DTXSID20553361;AKOS013498399;CS-0233303;EN300-132445

Suppliers and Price of 6-(Methylsulfanyl)hexan-1-amine

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
6-(Methylthio)-1-hexanamine
250mg
$ 160.00

Medical Isotopes, Inc.
6-(Methylthio)-1-hexanamine
2.5 g
$ 2200.00

AK Scientific
6-(Methylsulfanyl)hexan-1-amine
10g
$ 4004.00

AK Scientific
6-(Methylsulfanyl)hexan-1-amine
2.5g
$ 1897.00

Total 4 raw suppliers

Chemical Property of 6-(Methylsulfanyl)hexan-1-amine

Chemical Property:

PSA：51.32000
LogP:2.56880
XLogP3:1.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:6
Exact Mass:147.10817072
Heavy Atom Count:9
Complexity:48.2

Purity/Quality:

99% ^*data from raw suppliers

6-(Methylthio)-1-hexanamine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CSCCCCCCN
Uses 6-(Methylthio)-1-hexanamine is used as a reagent in the synthesis of diptocarpamine,a racemic alkaloid. 6-(Methylthio)-1-hexanamine may also have insulin-like activity.

Technology Process of 6-(Methylsulfanyl)hexan-1-amine

There total 19 articles about 6-(Methylsulfanyl)hexan-1-amine 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: 95.0%

: 125443-23-4
(6-azidohexyl)(methyl)sulfane

: 62580-22-7
7-thiaoctylamine

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether; for 0.333333h; Ambient temperature;
DOI:10.1007/BF00598411

Reference yield: 70.0%

: 117952-80-4
7-thiaoctyl isocyanate

: 62580-22-7
7-thiaoctylamine

Guidance literature:: With hydrogenchloride; In benzene; at 80 ℃; for 1h;
DOI:10.1007/BF00597577

Reference yield:

: 98433-41-1
6-(methylthio)hexan-1-ol

: 62580-22-7
7-thiaoctylamine

Guidance literature:: Multi-step reaction with 3 steps

1: 65 percent / PBr₃ / pyridine; diethyl ether / 1.) -30 deg C, 3h, 2.) 12h, 25 deg C

2: 56 percent / sodium azide / 2-ethoxy-ethanol; H₂O / 24 h / 90 °C

3: 95 percent / lithium tetrahydroaluminate / diethyl ether / 0.33 h / Ambient temperature

With lithium aluminium tetrahydride; sodium azide; phosphorus tribromide; In pyridine; 2-ethoxy-ethanol; diethyl ether; water;
DOI:10.1007/BF00598411