1-Adamantanecarboxamide

Base Information

Chemical Name:1-Adamantanecarboxamide
CAS No.:5511-18-2
Molecular Formula:C11H17NO
Molecular Weight:179.262
Hs Code.:29242990
European Community (EC) Number:640-514-8
DSSTox Substance ID:DTXSID30203628
Nikkaji Number:J55.145G
Wikidata:Q72436524
ChEMBL ID:CHEMBL2041315
Mol file:5511-18-2.mol

Synonyms:1-adamantanecarboxamide

Suppliers and Price of 1-Adamantanecarboxamide

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
1-Adamantanecarboxamide
10g
$ 1230.00

TRC
1-Adamantanecarboxamide
1g
$ 155.00

TCI Chemical
1-Adamantanecarboxamide >97.0%(GC)
5g
$ 133.00

TCI Chemical
1-Adamantanecarboxamide >97.0%(GC)
1g
$ 45.00

Sigma-Aldrich
1-Adamantanecarboxamide 97%
1g
$ 50.40

Oakwood
1-Adamantanecarboxamide 97%
250mg
$ 10.00

Matrix Scientific
Adamantane-1-carboxamide
5g
$ 174.00

Matrix Scientific
Adamantane-1-carboxamide
1g
$ 48.00

Frontier Specialty Chemicals
1-Adamantanecarboxamide
1g
$ 59.00

Frontier Specialty Chemicals
1-Adamantanecarboxamide
5g
$ 180.00

Total 57 raw suppliers

Chemical Property of 1-Adamantanecarboxamide

Chemical Property:

Appearance/Colour:white solid
Vapor Pressure:7.09E-05mmHg at 25°C
Melting Point:188-190 °C(lit.)
Refractive Index:1.572
Boiling Point:343.3 °C at 760 mmHg
PKA:16.85±0.20(Predicted)
Flash Point:161.4 °C
PSA：43.09000
Density:1.174 g/cm³
LogP:2.38840
Storage Temp.:Sealed in dry,Room Temperature
Solubility.:Chloroform, Dichloromethane, Methanol
XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:179.131014166
Heavy Atom Count:13
Complexity:218

Purity/Quality:

98% ^*data from raw suppliers

1-Adamantanecarboxamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:C1C2CC3CC1CC(C2)(C3)C(=O)N
Uses Reproduction of Sindbis virus strains sensitive and resistant to 1-adamantanecarboxamide

Technology Process of 1-Adamantanecarboxamide

There total 2 articles about 1-Adamantanecarboxamide 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: 61.0%

: 770-71-8
1-adamantanemethanol

: 23074-42-2
1-adamantanecarbonitrile

: 5511-18-2
adamantane-1-carboxamide

Guidance literature:: 1-adamantanemethanol; With ammonia; iodine; In water; at 60 ℃; for 6h;

With ammonia; dihydrogen peroxide; In water; at 0 - 20 ℃;
DOI:10.1016/j.tetlet.2010.06.051

Reference yield:

: 828-51-3
1-Adamantanecarboxylic acid

: 75-05-8,26809-02-9
acetonitrile

: adamantane-1-carboxylic acid acetyl-amide

: 23074-42-2
1-adamantanecarbonitrile

: 5511-18-2
adamantane-1-carboxamide

Guidance literature:: With sulfuric acid; at 40 ℃; for 18h;
DOI:10.1055/s-2005-871967

Reference yield: 99.0%

: 5511-18-2
adamantane-1-carboxamide

: 23074-42-2
1-adamantanecarbonitrile

Guidance literature:: With thiophosphorylated amine resin; 1-ethyl-3-methylimidazolium hexafluorophosphate; In toluene; at 200 ℃; for 0.25h; microwave irradiation;
DOI:10.1039/b008814p