| Identification | More | [Name]
N-Boc-L-alaninol | [CAS]
79069-13-9 | [Synonyms]
BOC-ALANINOL
BOC-ALA-OL
BOC-L-ALANINOL
BOC-L-ALA-OL
BOC-(S)-2-AMINO-1-PROPANOL
N-ALPHA-T-BOC-L-ALANINOL
N-ALPHA-TERT-BUTYLOXYCARBONYL-L-ALANINOL
N-BOC-L-ALANINOL
N-BOC-S-ALANINOL
N-T-BOC-L-ALANINOL
N-T-BUTOXYCARBONYL-L-ALANINOL
N-TERT-BUTOXYCARBONYL-L-ALANINOL
(S)-(-)-2-(BOC-AMINO)-1-PROPANOL
(S)-2-(BOC-AMINO)-1-PROPANOL
(S)-(-)-2-(TERT-BUTOXYCARBONYLAMINO)-1-PROPANOL
(S)-2-(TERT-BUTOXYCARBONYLAMINO)-1-PROPANOL
(S)-2-(TERT-BUTYLOXYCARBONYL-AMINO)-1-PROPANOL
TERT-BUTYL (1S)-2-HYDROXY-1-METHYLETHYLCARBAMATE
Boc-Ala-ol~(S)-2-(Boc-amino)-1-propanol~N-(tert-Butoxycarbonyl)-L-alaninol
Butoxycarbonylalaninol | [EINECS(EC#)]
807-439-4 | [Molecular Formula]
C8H17NO3 | [MDL Number]
MFCD00043121 | [Molecular Weight]
175.23 | [MOL File]
79069-13-9.mol |
| Chemical Properties | Back Directory | [Melting point ]
59-62 °C(lit.)
| [alpha ]
-11 º (c=1, chloroform) | [Boiling point ]
276.4±23.0 °C(Predicted) | [density ]
1.025±0.06 g/cm3(Predicted) | [refractive index ]
-8.6 ° (C=1.2, MeOH) | [storage temp. ]
2-8°C
| [solubility ]
almost transparency in Methanol | [form ]
Crystalline Powder or Lumps | [pka]
12.11±0.46(Predicted) | [color ]
White | [optical activity]
[α]20/D 11°, c = 1 in chloroform | [BRN ]
3648840 | [InChI]
InChI=1S/C8H17NO3/c1-6(5-10)9-7(11)12-8(2,3)4/h6,10H,5H2,1-4H3,(H,9,11)/t6-/m0/s1 | [InChIKey]
PDAFIZPRSXHMCO-LURJTMIESA-N | [SMILES]
C(OC(C)(C)C)(=O)N[C@@H](C)CO | [CAS DataBase Reference]
79069-13-9(CAS DataBase Reference) |
| Safety Data | Back Directory | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [F ]
9-21 | [HS Code ]
29051990 |
| Hazard Information | Back Directory | [Chemical Properties]
White to off-white powder | [Uses]
Boc-L-alanine (N-Boc-L-alaninol) is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a tert-butoxycarbonyl (Boc) protecting group, which enhances its stability and reactivity, making it an essential building block for the synthesis of various peptides and proteins. Its unique structure allows for selective deprotection under mild conditions, facilitating the production of complex molecules in a controlled manner.
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