N-Boc-L-valinol

Base Information

Chemical Name:N-Boc-L-valinol
CAS No.:79069-14-0
Molecular Formula:C10H21NO3
Molecular Weight:203.282
Hs Code.:29224999
European Community (EC) Number:626-744-1
DSSTox Substance ID:DTXSID70427366
Nikkaji Number:J1.183.382I
Wikidata:Q72451008
Mol file:79069-14-0.mol

Synonyms:N-Boc-L-valinol;Boc-L-valinol;79069-14-0;Boc-Valinol;(S)-N-(tert-Butoxycarbonyl)valinol;N-(tert-Butoxycarbonyl)-L-valinol;Boc-Val-ol;N-tert-Butoxycarbonyl-L-valinol;tert-butyl N-[(2S)-1-hydroxy-3-methylbutan-2-yl]carbamate;MFCD00082635;(S)-tert-butyl (1-hydroxy-3-methylbutan-2-yl)carbamate;(S)-tert-butyl 1-hydroxy-3-methylbutan-2-ylcarbamate;N-Boc-D-valinol;(R)-N-(tert-Butoxycarbonyl)valinol;BOC-D-VAL-OL;N-t-BOC-L-Valinol;n-tboc-l-valinol;Boc-ValCH2OH;(S)-2-(Boc-amino)-3-methyl-1-butanol;(s)-(-)-boc-valinol;SCHEMBL1134642;M-tert-Butoxycarbonyl-L-valinol;tert-butyl (S)-(1-hydroxy-3-methylbutan-2-yl)carbamate;DTXSID70427366;n-alpha-t-butyloxycarbonyl-l-valinol;(s)-n-(tert-butoxycarbonyl)-valinol;N-(tert.-butyloxycarbonyl)-L-valinol;AKOS005259784;AKOS015907104;CS-W015451;n-alpha-tert-butyloxycarbonyl-l-valinol;AC-24051;AS-14911;N-(tert-Butoxycarbonyl)-L-valinol, 96%;(s)-(-)-2-(boc-amino)-3-methyl-1-butanol;EN300-171458;(s)-2-(tertbutoxycarbonylamino)-3-methylbutanol;Q-101624;tert-Butyl 1-(hydroxymethyl)-2-methylpropylcarbamate #;tert-Butyl (1S)-1-(hydroxymethyl)-2-methylpropylcarbamate;1-Butanol, (Ss)-2-[(tert.butyloxycarbonyl)amino]-3-methyl-;((1S)-1-hydroxymethyl-2-methylpropyl)carbamic acid t-butyl ester;2-Methyl-2-propanyl [(2S)-1-hydroxy-3-methyl-2-butanyl]carbamate;1,1-dimethylethyl N-[1-(S)-(hydroxymethyl)-2-methylpropyl]carbamate;Carbamic acid, [(1S)-1-(hydroxymethyl)-2-methylpropyl]-, 1,1-dimethylethyl ester

Suppliers and Price of N-Boc-L-valinol

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
Boc-L-Valinol
2.5g
$ 75.00

SynQuest Laboratories
N-t-Boc-L-Valinol
5 g
$ 36.00

SynQuest Laboratories
N-t-Boc-L-Valinol
25 g
$ 103.00

Sigma-Aldrich
N-(tert-Butoxycarbonyl)-L-valinol 96%
5g
$ 208.00

Sigma-Aldrich
N-(tert-Butoxycarbonyl)-L-valinol 96%
1g
$ 58.10

Matrix Scientific
tert-Butyl (1S)-1-(hydroxymethyl)-2-methylpropylcarbamate 97%
10g
$ 656.00

Matrix Scientific
tert-Butyl (1S)-1-(hydroxymethyl)-2-methylpropylcarbamate 97%
1g
$ 102.00

Frontier Specialty Chemicals
N-Boc-L-valinol 98%
1g
$ 75.00

Crysdot
Boc-Valinol 97%
25g
$ 116.00

chempep
Boc-Valinol >=98%
5g
$ 323.00

Total 82 raw suppliers

Chemical Property of N-Boc-L-valinol

Chemical Property:

Appearance/Colour:Clear colorless to yellow liquid
Vapor Pressure:9.15E-05mmHg at 25°C
Refractive Index:n20/D 1.449(lit.)
Boiling Point:341.8 °C at 760 mmHg
PKA:12.02±0.46(Predicted)
Flash Point:160.5 °C
PSA：58.56000
Density:1.079 g/cm³
LogP:1.91890
Storage Temp.:Store at 0-5°C
XLogP3:1.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:203.15214353
Heavy Atom Count:14
Complexity:184

Purity/Quality:

99%, ^*data from raw suppliers

Boc-L-Valinol ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 26-36

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C(CO)NC(=O)OC(C)(C)C
Isomeric SMILES:CC(C)[C@@H](CO)NC(=O)OC(C)(C)C
Uses Starting material for the synthesis of enantiopure homo-β-amino acids. Used in the efficient synthesis of enantiopure tetrahydroisoquinolines. Intermediate in the one-pot conversion of amino acid carbamates to N-derivatized 2-oxazolidinones.

Technology Process of N-Boc-L-valinol

There total 44 articles about N-Boc-L-valinol 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: 100.0%