3-Aminobicyclo[2.2.1]heptane-2-carboxamide

Base Information

Chemical Name:3-Aminobicyclo[2.2.1]heptane-2-carboxamide
CAS No.:105786-39-8
Molecular Formula:C₈H₁₄N₂O
Molecular Weight:154.212
Hs Code.:2924297099
DSSTox Substance ID:DTXSID70547699
Mol file:105786-39-8.mol

Synonyms:3-aminobicyclo[2.2.1]heptane-2-carboxamide;3-aminonorbornane-2-carboxamide;1260670-34-5;SCHEMBL6078824;DTXSID70547699;105786-37-6;AKOS013666920;AB42806;SB74309;EN300-81871

Suppliers and Price of 3-Aminobicyclo[2.2.1]heptane-2-carboxamide

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

SynQuest Laboratories
diexo-3-Aminobicyclo[2.2.1]heptane-2-carboxylic acid amide
250 mg
$ 336.00

SynQuest Laboratories
diexo-3-Aminobicyclo[2.2.1]heptane-2-carboxylic acid amide
1 g
$ 1136.00

Apolloscientific
diexo-3-Amino-bicyclo[2.2.1]heptane-2-carboxylic acid amide
1g
$ 959.00

American Custom Chemicals Corporation
DIEXO-3-AMINO-BICYCLO(2.2.1)HEPTANE-2-CARBOXYLIC ACID AMIDE 95.00%
5MG
$ 497.20

Total 2 raw suppliers

Chemical Property of 3-Aminobicyclo[2.2.1]heptane-2-carboxamide

Chemical Property:

XLogP3:0.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:154.110613074
Heavy Atom Count:11
Complexity:193

Purity/Quality:

97% ^*data from raw suppliers

diexo-3-Aminobicyclo[2.2.1]heptane-2-carboxylic acid amide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC2CC1C(C2N)C(=O)N

Technology Process of 3-Aminobicyclo[2.2.1]heptane-2-carboxamide

There total 7 articles about 3-Aminobicyclo[2.2.1]heptane-2-carboxamide 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: 68.0%

: 105786-35-4
(rac-di-exo)-3-amino-bicyclo[2.2.1]heptane-2-carboxylic acid ethyl ester

: 105786-39-8
exo-3-aminobicyclo<2.2.1>heptane-exo-2-carboxamide

Guidance literature:: With ammonia; In methanol; for 336h;

Reference yield: 65.0%

: 3-(9H-fluoren-9-ylamino)bicyclo[2.2.1]heptane-2-carboxamide

: 105786-39-8
exo-3-aminobicyclo<2.2.1>heptane-exo-2-carboxamide

Guidance literature:: With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; at 0 ℃; for 2h;

Reference yield:

: (±)-exo-2-[N-(9H-fluoren-9-ylidene)]-4-oxo-2,3-diazatricyclo[4,3,1⁶'⁹,0]decane-2-ium-3-ide

: 105786-39-8
exo-3-aminobicyclo<2.2.1>heptane-exo-2-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium borohydride / methanol / 60 °C

2: 2,3-dicyano-5,6-dichloro-p-benzoquinone / tetrahydrofuran / 2 h / 0 °C

With potassium borohydride; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; methanol;