ChemicalBook > CAS DataBase List > N-Boc-L-Valinol

N-Boc-L-Valinol

Product Name
N-Boc-L-Valinol
CAS No.
79069-14-0
Chemical Name
N-Boc-L-Valinol
Synonyms
BOC-VAL-OL;BOC-VALINOL;BOC-L-VAL-OL;BOC-L-VALINOL;N-BOC-L-VALINOL;N-T-BOC-L-VALINOL;N-Boc-L-valinol,98%;(S)-(-)-BOC-VALINOL;N-BOC-L-Valinol,96%;N-ALPHA-T-BOC-L-VALINOL
CBNumber
CB8328616
Molecular Formula
C10H21NO3
Formula Weight
203.28
MOL File
79069-14-0.mol
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N-Boc-L-Valinol Property

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

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

Symbol(GHS)
Signal word
Warning
Hazard statements

H227Combustible liquid

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P403+P235Store in a well-ventilated place. Keep cool.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
444413
Product name
N-(tert-Butoxycarbonyl)-L-valinol
Purity
96%
Packaging
5g
Price
$123
Updated
2024/03/01
Sigma-Aldrich
Product number
444413
Product name
N-(tert-Butoxycarbonyl)-L-valinol
Purity
96%
Packaging
1g
Price
$69.9
Updated
2023/06/20
TRC
Product number
B673498
Product name
Boc-L-Valinol
Packaging
2.5g
Price
$75
Updated
2021/12/16
Frontier Specialty Chemicals
Product number
JK397463
Product name
N-Boc-L-valinol
Purity
98%
Packaging
1g
Price
$75
Updated
2021/12/16
AK Scientific
Product number
N125
Product name
Boc-L-Valinol
Packaging
1g
Price
$14
Updated
2021/12/16
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N-Boc-L-Valinol Chemical Properties,Usage,Production

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.

reaction suitability

reaction type: solution phase peptide synthesis

N-Boc-L-Valinol Preparation Products And Raw materials

Raw materials

Preparation Products

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N-Boc-L-Valinol Suppliers

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View Lastest Price from N-Boc-L-Valinol manufacturers

Sichuan HongRi Pharma-Tech Co.,Ltd
Product
Boc-L-Val-OL 79069-14-0
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
1T+
Release date
2024-01-14
Career Henan Chemical Co
Product
N-Boc-L-Valinol 79069-14-0
Price
US $200.00/KG
Min. Order
2KG
Purity
99%
Supply Ability
20kg
Release date
2018-07-30

79069-14-0, N-Boc-L-ValinolRelated Search:

TRISTEARIN Ketorolac tromethamine phytosphingosine Dexketoprofen trometamol Fosfomycin tromethamine (S)-(+)-2-Amino-3-methyl-1-butanol CARBONYL SULFIDE (R)-(-)-2-Amino-3-methyl-1-butanol 2-Chloro-2-methylpropane 1,1'-Carbonyldiimidazole DI-TERT-BUTYL ETHER Carbonyl iron powder NICKEL CARBONYL BOC-PEN(MOB)-OH N-Boc-L-valine N-Boc-L-tert-Leucine Boc-N-Methyl-L-isoleucine Boc-N-Me-Val-OH

  • 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
  • n-tert-butoxycarbonyl-(s)-2-amino-3-methyl-1-butanol
  • N-alpha-t-Butyloxycarbonyl-L-valinol, (S)-2-(t-Butyloxycarbonyl-amino)-3-methyl-1-butanol
  • (R)-2-BOC-3-METHYL-1-BUTANOL
  • (S)-N-(TERT-BUTOXYCARBONYL)VALINOL
  • (S)-(-)-BOC-VALINOL
  • (S)-(1-HYDROXYMETHYL-2-METHYL-PROPYL)-CARBAMIC ACID TERT-BUTYL ESTER
  • (S)-(-)-2-(BOC-AMINO)-3-METHYL-1-BUTANOL
  • (S)-2-(BOC-AMINO)-3-METHYL-1-BUTANOL
  • (S)-2-(TERT-BUTYLOXYCARBONYL-AMINO)-3-METHYL-1-BUTANOL
  • (S)-2-(TERT-BUTOXYCARBONYLAMINO)-3-METHYLBUTANOL
  • N-[(1S)-1-HYDROXYMETHYL-2-METHYLPROPYL]-CARBAMINSAURE-TERT-BUTYL ESTER
  • N-(TERT-BUTOXYCARBONYL)-L-VALINOL
  • N-T-BUTOXYCARBONYL-L-VALINOL
  • N-T-BOC-L-VALINOL
  • N-ALPHA-TERT-BUTYLOXYCARBONYL-L-VALINOL
  • N-ALPHA-T-BUTYLOXYCARBONYL-L-VALINOL
  • N-ALPHA-T-BOC-L-VALINOL
  • N-BOC-L-VALINOL
  • Carbamic acid, N-[(1S)-1-(hydroxymethyl)-2-methylpropyl]-, 1,1-dimethylethyl ester
  • N-BOC-L-Valinol,96%
  • (S)-tert-butyl (1-hydroxy-3-methylbutan-2-yl)carbamate
  • Boc-L-valinol≥ 98% (assay)
  • (R)-N-Boc-2-amino-1,1-diphenyl-1-propanol,99%e.e.
  • N-Boc-L-valinol,99%e.e.
  • N-Boc-L-Valinol USP/EP/BP
  • 79069-14-0
  • ALCOHOL
  • Amino Acid Derivatives
  • Amino Alcohols
  • Peptide Synthesis
  • Specialty Synthesis
  • Amino Acid Derivatives
  • Amino Alcohols
  • Peptide Synthesis
  • Amino Alcohols
  • Chiral Compound
  • Boc-Amino acid series
  • Amino Acids