(S)-2-Amino-4-methylpentan-1-ol hydrochloride

Base Information

Chemical Name:(S)-2-Amino-4-methylpentan-1-ol hydrochloride
CAS No.:17016-87-4
Molecular Formula:C₆H₁₅NO*ClH
Molecular Weight:153.652
Hs Code.:
DSSTox Substance ID:DTXSID501044484

Synonyms:(S)-2-Amino-4-methylpentan-1-ol hydrochloride;17016-87-4;(2S)-2-amino-4-methylpentan-1-ol;hydrochloride;leucinol hydrochlorid;H-Leu-ol.HCl;L-leucinol hydrochloric acid;(2S)-2-amino-4-methylpentan-1-ol hydrochloride;SCHEMBL7062675;ZVHVRRKOBBNFDU-RGMNGODLSA-N;DTXSID501044484;L-Leucinol hydrochloride, AldrichCPR;(S)-2-Amino-4-methylpentan-1-olhydrochloride;EN300-303748;A811175;(2S)-2-Amino-4-methyl-1-pentanol hydrochloride (1:1)

Suppliers and Price of (S)-2-Amino-4-methylpentan-1-ol hydrochloride

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 6 raw suppliers

Chemical Property of (S)-2-Amino-4-methylpentan-1-ol hydrochloride

Chemical Property:

Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:153.0920418
Heavy Atom Count:9
Complexity:54.5

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)CC(CO)N.Cl
Isomeric SMILES:CC(C)C[C@@H](CO)N.Cl

Technology Process of (S)-2-Amino-4-methylpentan-1-ol hydrochloride

There total 5 articles about (S)-2-Amino-4-methylpentan-1-ol hydrochloride 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: 65.0%

: 7533-40-6,14438-11-0
(S)-2-amino-4-methylpentan-1-ol

: 17016-87-4,17016-88-5
(S)-leucinol hydrochloride

Guidance literature:: With manganese(II) chloride tetrahydrate; In chlorobenzene; for 40h; Reflux;

Reference yield:

: 3183-10-6
N-phthalimide-L-leucinyl chloride

: 17016-87-4,17016-88-5
(S)-leucinol hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: H₂ / 5percent Pd/BaSO₄ / xylene / 6 h / 110 °C

2: NaBH₄ / ethanol / 0.5 h / 4 °C

3: conc. HCl / dioxane / 24 h / Heating

With hydrogenchloride; sodium tetrahydroborate; hydrogen; Pd-BaSO₄; In 1,4-dioxane; ethanol; xylene;
DOI:10.1021/jm00347a024

Reference yield:

: 2419-38-7
N-phthaloyl-(S)-leucine

: 17016-87-4,17016-88-5
(S)-leucinol hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1: SOCl₂ / benzene / 6 h / Heating

2: H₂ / 5percent Pd/BaSO₄ / xylene / 6 h / 110 °C

3: NaBH₄ / ethanol / 0.5 h / 4 °C

4: conc. HCl / dioxane / 24 h / Heating

With hydrogenchloride; sodium tetrahydroborate; thionyl chloride; hydrogen; Pd-BaSO₄; In 1,4-dioxane; ethanol; xylene; benzene;
DOI:10.1021/jm00347a024