4-(Tricyclo[3.3.1.13,7]dec-1-ylsulfanyl)aniline

Base Information

Chemical Name:4-(Tricyclo[3.3.1.13,7]dec-1-ylsulfanyl)aniline
CAS No.:56714-88-6
Molecular Formula:C16H21NS
Molecular Weight:259.415
Hs Code.:
NSC Number:111654
DSSTox Substance ID:DTXSID10296811
Wikidata:Q82037592
ChEMBL ID:CHEMBL1998672

Synonyms:56714-88-6;4-(tricyclo[3.3.1.13,7]dec-1-ylsulfanyl)aniline;NSC111654;CHEMBL1998672;SCHEMBL11447125;DTXSID10296811;NSC-111654

Suppliers and Price of 4-(Tricyclo[3.3.1.13,7]dec-1-ylsulfanyl)aniline

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

Total 4 raw suppliers

Chemical Property of 4-(Tricyclo[3.3.1.13,7]dec-1-ylsulfanyl)aniline

Chemical Property:

Vapor Pressure:2.83E-07mmHg at 25°C
Boiling Point:420.4°Cat760mmHg
Flash Point:208°C
Density:1.19g/cm³
XLogP3:4.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:259.13947085
Heavy Atom Count:18
Complexity:278

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C2CC3CC1CC(C2)(C3)SC4=CC=C(C=C4)N

Technology Process of 4-(Tricyclo[3.3.1.13,7]dec-1-ylsulfanyl)aniline

There total 4 articles about 4-(Tricyclo[3.3.1.13,7]dec-1-ylsulfanyl)aniline 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: 56.0%

: 768-90-1
1-Adamantyl bromide

: 1193-02-8
4-aminotiophenol

: 56714-88-6
p(1-Adamantylthio)aniline

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 20 ℃; for 48h; Inert atmosphere;

Reference yield:

: 56714-87-5
1-adamantyl (4-nitro)phenyl sulfide

: 56714-88-6
p(1-Adamantylthio)aniline

Guidance literature:: With hydrogen; palladium on activated charcoal;
DOI:10.1021/jm00187a016

Reference yield:

: 350-46-9,178603-76-4
4-Fluoronitrobenzene

: 56714-88-6
p(1-Adamantylthio)aniline

Guidance literature:: Multi-step reaction with 2 steps

1: (i) NaH, DMF, (ii) /BRN= 606923/

2: H₂ / Pd-C

With hydrogen; palladium on activated charcoal;
DOI:10.1021/jm00187a016