| Identification | More | [Name]
N-Boc-L-Valinol | [CAS]
79069-14-0 | [Synonyms]
BOC-L-VALINOL
BOC-L-VAL-OL
BOC-(S)-2-AMINO-3-METHYL-1-BUTANOL
BOC-VALINOL
BOC-VAL-OL
N-[(1S)-1-HYDROXYMETHYL-2-METHYLPROPYL]-CARBAMINSAURE-TERT-BUTYL ESTER
N-ALPHA-T-BOC-L-VALINOL
N-ALPHA-T-BUTYLOXYCARBONYL-L-VALINOL
N-ALPHA-TERT-BUTYLOXYCARBONYL-L-VALINOL
N-BOC-L-VALINOL
N-T-BOC-L-VALINOL
N-T-BUTOXYCARBONYL-L-VALINOL
N-(TERT-BUTOXYCARBONYL)-L-VALINOL
(R)-2-BOC-3-METHYL-1-BUTANOL
(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-BUTOXYCARBONYLAMINO)-3-METHYLBUTANOL
(S)-2-(TERT-BUTYLOXYCARBONYL-AMINO)-3-METHYL-1-BUTANOL
(S)-(-)-BOC-VALINOL | [Molecular Formula]
C10H21NO3 | [MDL Number]
MFCD00082635 | [Molecular Weight]
203.28 | [MOL File]
79069-14-0.mol |
| Chemical Properties | Back Directory | [Appearance]
Clear colorless to yellow liquid | [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.)
| [Fp ]
185 °F
| [storage temp. ]
Store at 0-5°C | [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) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [RIDADR ]
NA 1993 / PGIII | [WGK Germany ]
3
| [HS Code ]
29224999 |
| Hazard Information | Back Directory | [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 |
|
|