| Identification | More | [Name]
N-(tert-Butoxycarbonyl)-L-alanine | [CAS]
15761-38-3 | [Synonyms]
BOC-ALA
BOC-ALANINE
BOC-ALA-OH
BOC-L-ALA
BOC-L-ALANINE
BOC-L-ALANINE-OH
BOC-L-ALA-OH
H-ALPHA-T-BOC-L-ALANINE
L-ALANINE, N-[(1,1-DIMETHYLETHOXY)CARBONYL]-
N-[(1,1-Dimethylethoxy)carbonyl]-L-alanine
N-ALPHA-T-BOC-L-ALANINE
N-ALPHA-T-BUTYLOXYCARBONYL-L-ALANINE
N-ALPHA-TERT-BUTYLOXYCARBONYL-L-ALANINE
N-BOC-L-ALANINE
N-T-BOC-L-ALANINE
N-(T-BUTOXYCARBONYL)-L-ALANINE
N-(TERT-BUTOXYCARBONYL)-L-ALANINE
N-(TERT-BUTOXYEARBONYL)-L-ALANINE
TBOC-L-ALANINE
T-BUTYLOXYCARBONYL-L-ALANINE | [EINECS(EC#)]
239-847-8 | [Molecular Formula]
C8H15NO4 | [MDL Number]
MFCD00037225 | [Molecular Weight]
189.21 | [MOL File]
15761-38-3.mol |
| Chemical Properties | Back Directory | [Appearance]
White to off-white microcrystalline powder | [Melting point ]
79-83 °C(lit.) | [alpha ]
-26 º (c=2, acetic acid) | [Boiling point ]
324.46°C (rough estimate) | [density ]
1.2321 (rough estimate) | [refractive index ]
-25.5 ° (C=2, AcOH) | [storage temp. ]
−20°C
| [solubility ]
DMSO, Methanol | [form ]
Granular Powder | [pka]
4.02±0.10(Predicted) | [color ]
White | [optical activity]
[α]20/D 25±1°, c = 2% in acetic acid | [Detection Methods]
T,NMR | [BRN ]
1726365 | [CAS DataBase Reference]
15761-38-3(CAS DataBase Reference) | [EPA Substance Registry System]
15761-38-3(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi,Xn | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S24/25:Avoid contact with skin and eyes .
S36:Wear suitable protective clothing .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [TSCA ]
Yes | [HazardClass ]
IRRITANT | [HS Code ]
29241990 |
| Hazard Information | Back Directory | [Chemical Properties]
White to off-white microcrystalline powder | [Uses]
Boc-Ala-OH can be used:
- In the preparation of N-propargylalanine, a key precursor to generate N-(3-aryl)propylated alanine residues.
- In the resolution of racemic mixture of 3,3′-bis(benzyloxy)-1,1′-binaphthalene-2,2′-diol.
- In the one-pot synthesis of hybrid tripeptidomimetics containing both amide and imide functionalities.
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