1-NITROADAMANTANE

Base Information

Chemical Name:1-NITROADAMANTANE
CAS No.:7575-82-8
Molecular Formula:C10H15NO2
Molecular Weight:181.235
Hs Code.:
Mol file:7575-82-8.mol

Synonyms:Adamantane,1-nitro- (6CI,7CI,8CI);1-Nitroadamantane;NSC 130990;NSC 235788;

Suppliers and Price of 1-NITROADAMANTANE

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-Nitroadamantane
10g
$ 1165.00

Medical Isotopes, Inc.
1-Nitroadamantane
1 g
$ 620.00

Matrix Scientific
1-Nitroadamantane
500mg
$ 119.00

Crysdot
1-Nitroadamantane 95+%
5g
$ 535.00

Chemenu
1-Nitroadamantane 95%
5g
$ 505.00

American Custom Chemicals Corporation
1-NITROADAMANTANE 95.00%
5MG
$ 505.93

AK Scientific
1-Nitroadamantane
500mg
$ 210.00

aablocks
1-Nitroadamantane 95%
25g
$ 1756.00

aablocks
1-Nitroadamantane 95%
5g
$ 456.00

aablocks
1-Nitroadamantane 95%
1g
$ 135.00

Total 25 raw suppliers

Chemical Property of 1-NITROADAMANTANE

Chemical Property:

Vapor Pressure:0.00463mmHg at 25°C
Melting Point:159℃
Refractive Index:1.545
Boiling Point:277.1 °C at 760 mmHg
Flash Point:121.8 °C
PSA：45.82000
Density:1.19 g/cm³
LogP:2.75510
Storage Temp.:-20°C Freezer, Under inert atmosphere
Solubility.:Chloroform (Slightly), Methanol (Sparingly)

Purity/Quality:

97% ^*data from raw suppliers

1-Nitroadamantane ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses 1-Nitroadamantane is a biologically active polycycloalkane that exhibits antiviral activities and as well as inhibitory activities towards the poliferation of lymphocytes.

Technology Process of 1-NITROADAMANTANE

There total 22 articles about 1-NITROADAMANTANE 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: 90.0%

: 281-23-2
adamantane

: 768-95-6
1-adamanthanol

: 7575-82-8
1-nitroadamantane

: 32314-61-7
1-nitroxyadamantane

Guidance literature:: With Nitrogen dioxide; ozone; In dichloromethane; at -78 ℃; for 0.5h;
DOI:10.1039/cc9960001783

Reference yield: 74.0%

: 281-23-2
adamantane

: 768-92-3
1-adamantyl fluoride

: 58652-35-0
1-hydroxy-3-fluoroadamante

: 768-95-6
1-adamanthanol

: 7575-82-8
1-nitroadamantane

Guidance literature:: With nitronium tetrafluoborate; In various solvent(s); Further byproducts given; Ambient temperature;

Reference yield: 66.2%

: 281-23-2
adamantane

: 700-58-3
2-Adamantanone

: 768-92-3
1-adamantyl fluoride

: 58652-35-0
1-hydroxy-3-fluoroadamante

: 768-95-6
1-adamanthanol

: 7575-82-8
1-nitroadamantane

Guidance literature:: With nitronium tetrafluoborate; In nitromethane; Mechanism; Ambient temperature; var. solvent; kinetic hydrogen isotope effect with 1,3,5,7-tetradeuterioadamantane;