N-Boc-L-alaninol , 98% , 79069-13-9

Synonym(s):
(S)-(−)-2-(tert-Butoxycarbonylamino)-1-propanol;N-Boc-L-alaninol;Boc-L-alaninol

CAS NO.：79069-13-9

Empirical Formula: C8H17NO3

Molecular Weight: 175.23

MDL number: MFCD00043121

EINECS: 807-439-4

PRODUCT Properties

• 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.: Sealed in dry,2-8°C
• solubility: almost transparency in Methanol
• pka: 12.11±0.46(Predicted)
• form: Crystalline Powder or Lumps
• 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)

Description and 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.

Safety

• Symbol(GHS): GHS07
• Signal word: Warning
• Hazard statements: H315-H319-H335
• Precautionary statements: P261-P271-P280
• Safety Statements: 22-24/25
• WGK Germany: 3
• F: 9-21
• HS Code: 29051990