2-Amino-3-hexanol

Base Information

Chemical Name:2-Amino-3-hexanol
CAS No.:13325-11-6
Molecular Formula:C6H15NO
Molecular Weight:117.1894
Hs Code.:
NSC Number:17699
DSSTox Substance ID:DTXSID70928020
Nikkaji Number:J73.724K

Synonyms:2-Amino-3-hexanol;USAF CS-2;13325-11-6;3-HEXANOL, 2-AMINO-;NSC 17699;2-aminohexan-3-ol;NSC17699;WLN: ZY1&YQ3;SCHEMBL2100071;DTXSID70928020;NSC-17699;AKOS006340329;LS-75379

Suppliers and Price of 2-Amino-3-hexanol

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

Total 3 raw suppliers

Chemical Property of 2-Amino-3-hexanol

Chemical Property:

Vapor Pressure:0.0564mmHg at 25°C
Boiling Point:206.3°Cat760mmHg
Flash Point:78.6°C
Density:0.904g/cm³
XLogP3:0.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:117.115364102
Heavy Atom Count:8
Complexity:56.5

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCC(C(C)N)O

Technology Process of 2-Amino-3-hexanol

There total 3 articles about 2-Amino-3-hexanol 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:

: 5448-00-0
2-nitro-hexan-3-ol

: 13325-11-6
2-amino-hexan-3-ol

Guidance literature:: With acetic acid; isopropyl alcohol; zinc;
DOI:10.1021/jo01137a019

Reference yield:

: 10021-63-3
(R)-(+)-2-hydroxypentanenitrile

: 13325-11-6,131298-20-9
(1R,2R)-2-Amino-3-hexanol

Guidance literature:: Multi-step reaction with 2 steps

1: 63 percent / pyridine / 4 h / Ambient temperature

2: 2) NaBH₄ / 1) Et₂O, 12 h, room temperature, 2) THF, MeOH, -50 deg C, 4 h

With pyridine; sodium tetrahydroborate;

Reference yield:

: 917-64-6
methyl magnesium iodide

: 131298-17-4
(R)-2-(Trimethylsiloxy)pentannitril

: 131298-20-9
erythro-(2S,3R)-2-aminohexan-3-ol

: 13325-11-6,131298-20-9
(1R,2R)-2-Amino-3-hexanol

Guidance literature:: With sodium tetrahydroborate; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts; 1) Et₂O, 12 h, room temperature, 2) THF, MeOH, -50 deg C, 4 h;