8-Benzyl-3a-amino-1aH,5aH-nortropane

Base Information Edit

Chemical Name:8-Benzyl-3a-amino-1aH,5aH-nortropane
CAS No.:76272-36-1
Molecular Formula:C14H20N2
Molecular Weight:216.326
Hs Code.:2933990090
European Community (EC) Number:616-315-7,840-452-3
UNII:7FK5A8SQ6H,P234Y64DRA
DSSTox Substance ID:DTXSID801191321
Wikidata:Q76416495
Mol file:76272-36-1.mol

Synonyms:76272-35-0;8-Benzyl-3a-amino-1aH,5aH-nortropane;endo-8-Benzyl-8-azabicyclo[3.2.1]octan-3-amine;(1R,5S)-endo-8-Benzyl-8-azabicyclo[3.2.1]octan-3-amine;8-Benzyl-8-azabicyclo[3.2.1]octan-3-exo-amine;(1R,5S)-8-benzyl-8-azabicyclo[3.2.1]octan-3-amine;(1S,5R)-8-benzyl-8-azabicyclo[3.2.1]octan-3-amine;(3-ENDO)-8-(PHENYLMETHYL)-8-AZABICYCLO[3.2.1]OCTAN-3-AMINE;EXO-3-AMINO-8-BENZYL-8-AZABICYCLO[3.2.1]OCTANE;3-AMINO-8-BENZYL-8-AZABICYCLO[3.2.1]OCTANE;7FK5A8SQ6H;8-Benzyl-8-azabicyclo[3.2.1]octane-3-endo-amine;SCHEMBL168286;P234Y64DRA;SCHEMBL15021133;SCHEMBL21772974;(1R,5S)-endo-8-Benzyl-8-azabicyclo-[3.2.1]octan-3-amine;DTXSID801191321;AMY12569;WDA90192;MFCD08460051;AKOS015920257;AKOS017344555;AKOS037644325;DS-1433;AS-50630;CS-0003872;CS-0022861;P10756;8-Benzyl-3alpha-amino-1alphaH,5alphaH-nortropane;A865516;exo 8-Benzyl-8-azabicyclo[3.2.1]octan-3-amine;(3-exo)-8-(Phenylmethyl)-8-azabicyclo[3.2.1]octan-3-amine;8-Azabicyclo[3.2.1]octan-3-amine,8-(phenylmethyl)-,endo-;(1R,3S,5S)-8-BENZYL-8-AZABICYCLO[3.2.1]OCTAN-3-AMINE;8-Azabicyclo[3.2.1]octan-3-amine, 8-(phenylmethyl)-, (3-endo)-;8-Azabicyclo[3.2.1]octan-3-amine;8-(phenylmethyl)-endo-3-AMINO-8-BENZYL-8-AZABICYCLO[3.2.1]OCTANE (3-ENDO)-8-BENZYL-3A-AMINO-1AH5AH-NORTROPANE

Suppliers and Price of 8-Benzyl-3a-amino-1aH,5aH-nortropane

Supply Marketing:Edit

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
Benzyl-8-azabicyclo[3.2.1]octan-3-exo-amine
500mg
$ 165.00

Synthonix
exo-3-Amino-8-benzyl-8-azabicyclo[3.2.1]octane 95+%
1g
$ 160.00

Matrix Scientific
8-Benzyl-8-azabicyclo[3.2.1]octan-3-exo-amine 95+%
1g
$ 700.00

Matrix Scientific
8-Benzyl-8-azabicyclo[3.2.1]octan-3-exo-amine 95+%
5g
$ 1750.00

Matrix Scientific
8-Benzyl-8-azabicyclo[3.2.1]octan-3-exo-amine 95+%
250mg
$ 324.00

Chemenu
exo-8-Benzyl-8-azabicyclo[3.2.1]octan-3-amine 95%
1g
$ 102.00

Chemenu
exo-8-Benzyl-8-azabicyclo[3.2.1]octan-3-amine 95%
5g
$ 281.00

Chemenu
exo-8-Benzyl-8-azabicyclo[3.2.1]octan-3-amine 95%
10g
$ 468.00

Biosynth Carbosynth
Benzyl-8-azabicyclo[3.2.1]octan-3-exo-amine
500 mg
$ 1530.00

Biosynth Carbosynth
Benzyl-8-azabicyclo[3.2.1]octan-3-exo-amine
250 mg
$ 840.00

Total 50 raw suppliers

Chemical Property of 8-Benzyl-3a-amino-1aH,5aH-nortropane Edit

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Refractive Index:1.581
Boiling Point:317.1 °C at 760 mmHg
PKA:10.23±0.20(Predicted)
Flash Point:133.4 °C
PSA：29.26000
Density:1.082 g/cm³
LogP:2.77890
Storage Temp.:under inert gas (nitrogen or Argon) at 2–8 °C
Solubility.:Chloroform (Slightly), Methanol (Slightly)
XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:216.162648646
Heavy Atom Count:16
Complexity:221

Purity/Quality:

98%,99%, ^*data from raw suppliers

Benzyl-8-azabicyclo[3.2.1]octan-3-exo-amine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC2CC(CC1N2CC3=CC=CC=C3)N
Isomeric SMILES:C1C[C@H]2CC(C[C@@H]1N2CC3=CC=CC=C3)N
Uses Intermediate in the preparation of CCR5 receptor antagonists, antibacterial agents and dopamine antagonists

Technology Process of 8-Benzyl-3a-amino-1aH,5aH-nortropane

There total 20 articles about 8-Benzyl-3a-amino-1aH,5aH-nortropane 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: 100.0%