BOC-ALA-ALA-OH

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CAS:27317-69-7
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BOC-ALA-ALA-OH manufacturers

  • Boc-Ala-Ala-OH
  • Boc-Ala-Ala-OH pictures
  • 2026-08-18
  • CAS:27317-69-7
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 1T+
  • BOC-ALA-ALA-OH
  • BOC-ALA-ALA-OH pictures
  • 2025-04-04
  • CAS:27317-69-7
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 1Ton
BOC-ALA-ALA-OH Basic information
Product Name:BOC-ALA-ALA-OH
Synonyms:BOC-ALA-ALA-OH;BOC-ALA-ALA-OH H2O;BOC-L-ALANYL-L-ALANINE H2O;BOC-L-ALANYL-L-ALANINE MONOHYDRATE;N-tert-Butoxycarbonyl-L-alanyl-L-alanine;Boc-AA-OH;Boc-L-Ala-L-Ala-OH;L-Alanine,N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl-
CAS:27317-69-7
MF:C11H20N2O5
MW:260.29
EINECS:421-060-8
Product Categories:
Mol File:27317-69-7.mol
BOC-ALA-ALA-OH Structure
BOC-ALA-ALA-OH Chemical Properties
Melting point 132-133 °C
Boiling point 483.5±30.0 °C(Predicted)
density 1.163±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,2-8°C
solubility DMSO (Slightly), Methanol (Slightly)
pka3.52±0.10(Predicted)
form Solid
color White to Off-White
Stability:Hygroscopic
InChI1S/C11H20N2O5/c1-6(8(14)12-7(2)9(15)16)13-10(17)18-11(3,4)5/h6-7H,1-5H3,(H,12,14)(H,13,17)(H,15,16)/t6-,7-/m0/s1
InChIKeyBZNDDHWTEVCBAD-BQBZGAKWSA-N
SMILESC[C@H](NC(=O)[C@H](C)NC(=O)OC(C)(C)C)C(O)=O
Safety Information
WGK Germany WGK 3
Storage Class11 - Combustible Solids
MSDS Information
BOC-ALA-ALA-OH Usage And Synthesis
UsesN-Phthalyl-alanine is used in the preparation of endothiopeptide inhibitors of HIV-1 Protease.
Synthesis
L-Alanyl-L-alanine

1948-31-8

Di-tert-butyl dicarbonate

24424-99-5

BOC-ALA-ALA-OH

27317-69-7

GENERAL STEPS: L-alanyl-L-alanine (1 mmol) was slowly added to a solution of ethanol (1 mL) containing guanidine hydrochloride (15 mmol) and di-tert-butyl dicarbonate (2.5-3 mmol) under stirring conditions, maintaining the reaction temperature at 35-40°C. The reaction mixture was stirred continuously until a clarified solution was formed. Subsequently, the ethanol was removed by evaporation under reduced pressure. The residue was washed sequentially with distilled water (2 mL) and hexane or petroleum ether (2 mL) to obtain nearly pure N-tert-butoxycarbonyl-alanylalanine. If further product purity is required, the crude product can be purified by recrystallization.

References[1] Journal of Organic Chemistry, 2007, vol. 72, # 2, p. 525 - 531
[2] Journal of the American Chemical Society, 2000, vol. 122, # 12, p. 2687 - 2697
[3] Journal of Organic Chemistry, 1994, vol. 59, # 19, p. 5784 - 5793
[4] Tetrahedron Letters, 2011, vol. 52, # 12, p. 1260 - 1264
[5] Journal of Medicinal Chemistry, 2005, vol. 48, # 16, p. 5305 - 5320
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