(1-Adamantylamino)acetonitrile

Base Information

Chemical Name:(1-Adamantylamino)acetonitrile
CAS No.:16782-40-4
Molecular Formula:C₁₂H₁₈N₂
Molecular Weight:190.288
Hs Code.:
DSSTox Substance ID:DTXSID701233239
Mol file:16782-40-4.mol

Synonyms:(1-adamantylamino)acetonitrile;16782-40-4;2-(1-adamantylamino)acetonitrile;2-[(adamantan-1-yl)amino]acetonitrile;(1-adamantyl)aminoacetonitrile;DTXSID701233239;MFCD09063113;STK665357;AKOS000251590;AKOS006344023;LS-03505;AJ-264/34032057;(tricyclo[3.3.1.1~3,7~]dec-1-ylamino)acetonitrile;2-(Tricyclo[3.3.1.13,7]dec-1-ylamino)acetonitrile

Suppliers and Price of (1-Adamantylamino)acetonitrile

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

Matrix Scientific
(1-Adamantylamino)acetonitrile
500mg
$ 237.00

Biosynth Carbosynth
(1-Adamantylamino)acetonitrile
500 mg
$ 150.00

Biosynth Carbosynth
(1-Adamantylamino)acetonitrile
250 mg
$ 85.00

Biosynth Carbosynth
(1-Adamantylamino)acetonitrile
2 g
$ 434.00

Biosynth Carbosynth
(1-Adamantylamino)acetonitrile
1 g
$ 255.00

Biosynth Carbosynth
(1-Adamantylamino)acetonitrile
5 g
$ 868.00

AK Scientific
(1-Adamantylamino)acetonitrile
2g
$ 635.00

AK Scientific
(1-Adamantylamino)acetonitrile
500mg
$ 252.00

Total 4 raw suppliers

Chemical Property of (1-Adamantylamino)acetonitrile

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:190.146998583
Heavy Atom Count:14
Complexity:245

Purity/Quality:

97% ^*data from raw suppliers

(1-Adamantylamino)acetonitrile ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C2CC3CC1CC(C2)(C3)NCC#N

Technology Process of (1-Adamantylamino)acetonitrile

There total 3 articles about (1-Adamantylamino)acetonitrile 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: 89.0%

: 624-75-9
iodoacetonitrile

: 768-94-5
1-Adamantanamine

: 16782-40-4
(1-adamantyl)aminoacetonitrile

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 1h;
DOI:10.1055/s-2000-6428

Reference yield: 4.0%

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: 768-94-5
1-Adamantanamine

: 16782-40-4
(1-adamantyl)aminoacetonitrile

: 1-(1-adamantyl)diaziridine

Guidance literature:: With N-benzyl-N,N,N-triethylammonium chloride; potassium carbonate; hydroxylamine-O-sulfonic acid; In diethyl ether; chloroform; water; at 30 - 35 ℃; for 12h;
DOI:10.1007/BF02495223