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N-Boc-L-Valinol

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N-Boc-L-Valinol Basic information

Product Name:
N-Boc-L-Valinol
Synonyms:
  • Boc-Val-ol~N-tert-Butoxycarbonyl-(S)-2-amino-3-methyl-1-butanol~N-(tert-Butoxycarbonyl)-L-valinol
  • BOC-(S)-2-AMINO-3-METHYL-1-BUTANOL
  • BOC-VAL-OL
  • BOC-VALINOL
  • BOC-L-VAL-OL
  • BOC-L-VALINOL
  • N-Boc-L-valinol,98%
  • Carbamic acid, (1S)-1-(hydroxymethyl)-2-methylpropyl-, 1,1-dimethylethyl ester
CAS:
79069-14-0
MF:
C10H21NO3
MW:
203.28
Product Categories:
  • Amino Acid Derivatives
  • Amino Alcohols
  • Amino Alcohols
  • Chiral Compound
  • Boc-Amino acid series
  • Peptide Synthesis
  • Amino Acids
Mol File:
79069-14-0.mol
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N-Boc-L-Valinol Chemical Properties

alpha 
-23 º (c=1 in chloroform)
Boiling point:
208 °C(lit.)
Density 
0.995 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.449(lit.)
Flash point:
185 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form 
Powder
pka
12.02±0.46(Predicted)
optical activity
[α]23/D 23°, c = 1 in chloroform
BRN 
4663728
CAS DataBase Reference
79069-14-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
NA 1993 / PGIII
WGK Germany 
3
HS Code 
29224999

MSDS

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N-Boc-L-Valinol Usage And Synthesis

Chemical Properties

Clear colorless to yellow liquid

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.

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