| 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 Rotation]
[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 | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H315-H319-H335 | [Precautionary statements ]
P261-P271-P280 | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [F ]
9-21 | [REACH Registrations]
Active | [HS Code ]
29051990 | [Storage Class]
11 - Combustible Solids |
| 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.
| [Synthesis]
N-Boc-L-alaninol can be prepared from L-alanine by successive esterification, protection and reduction.
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| Company Name: |
SHENZHEN REISCH BIOTECH CO., LTD Gold
|
| Telephone: |
0755-0755-28609002 15112530219 |
| Website: |
https://www.chemicalbook.com/ShowSupplierProductsList231967/0_EN.htm |
| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Alfa Aesar
|
| Telephone: |
400-6106006 |
| Website: |
http://chemicals.thermofisher.cn |
| Company Name: |
Energy Chemical
|
| Telephone: |
400-0056266 |
| Website: |
www.energy-chemical.com |
|