3-Aminononan-2-ol

Base Information

Chemical Name:3-Aminononan-2-ol
CAS No.:75166-64-2
Molecular Formula:C9H21 N O
Molecular Weight:159.272
Hs Code.:
European Community (EC) Number:278-091-3
NSC Number:272454
DSSTox Substance ID:DTXSID90965997
Nikkaji Number:J349.502G
Mol file:75166-64-2.mol

Synonyms:3-Aminononan-2-ol;75166-64-2;3-amino-2-nonanol;51714-10-4;EINECS 278-091-3;NSC272454;SCHEMBL1742708;DTXSID90965997;NSC-272454;FT-0661966;FT-0661967

Suppliers and Price of 3-Aminononan-2-ol

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
3-Aminononan-2-ol
2.5g
$ 1435.00

TRC
3-Aminononan-2-ol
1g
$ 670.00

Total 6 raw suppliers

Chemical Property of 3-Aminononan-2-ol

Chemical Property:

Vapor Pressure:0.00157mmHg at 25°C
Boiling Point:262.2°C at 760 mmHg
Flash Point:112.4°C
Density:0.889g/cm³
XLogP3:2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:6
Exact Mass:159.162314293
Heavy Atom Count:11
Complexity:85.6

Purity/Quality:

99% ^*data from raw suppliers

3-Aminononan-2-ol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCC(C(C)O)N
Uses 3-Aminononan-2-ol is an intermediate in the synthesis of rac erythro-9-(2-Hydroxy-3-nonyl)adenine Hydrochloride Salt (H825550), which is a potent inhibitor of phosphodiesterase II (PDE II) (IC50=800nM). Does not inhibit other PDE isozymes (IC50>100uM). Inhibits the retrograde transport motor, dynein. Also inhibits adenosine deaminase (Ki=4nM). Potent PDE-2 inhibitor.

Technology Process of 3-Aminononan-2-ol

There total 6 articles about 3-Aminononan-2-ol 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: 75.0%

: 75166-64-2
3-aminononan-2-ol

Guidance literature:

Reference yield:

: 51714-08-0
3-aminononan-2-one hydrochloride

: 75166-64-2
3-aminononan-2-ol

Guidance literature:: With potassium borohydride;

Reference yield:

: 103539-11-3,103664-97-7
(S)-3-((R)-2-Hydroxy-1-phenyl-ethylamino)-nonan-2-ol

: 51714-10-4,51714-13-7,75166-64-2,79854-85-6,79854-86-7,79854-87-8,79854-88-9,87935-58-8,119720-60-4
(S)-3-Amino-nonan-2-ol

Guidance literature:: With hydrogen; palladium dihydroxide; In methanol; for 12h; under 760 Torr; Yield given; Ambient temperature;
DOI:10.1016/S0040-4039(01)84595-0