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ChemicalBook--->CAS DataBase List--->3392-05-0

3392-05-0

3392-05-0 Structure

3392-05-0 Structure
IdentificationMore
[Name]

Succinimido (S)-2-[(tert-butoxycarbonyl)amino]propionate
[CAS]

3392-05-0
[Synonyms]

BOC-D-ALANINE-HYDROXYSUCCINIMIDE ESTER
BOC-D-ALANINE N-HYDROXYSUCCINIMIDE ESTER
BOC-D-ALANINE-OSU
BOC-D-ALA-OSU
N-ALPHA-T-BOC-D-ALANINE N-HYDROXYSUCCINIMIDE ESTER
succinimido (S)-2-[(tert-butoxycarbonyl)amino]propionate
Boc-L-Alanine N-hydroxysuccinimde ester
BOC-L-ALA-OSU
Boc-L-alanineydroxysuccinimidester
Boc-Ala-OSu
Boc-L-alanine N-succinimidyl ester
BOC-ALANINE-1-HYDROXYSUCCINIMIDE ESTER
BOC-L-ALANINE-HYDROXYSUCCINIMIDESTER
N-(tert-butoxycarbonyl)-L-alanine hydroxysuccinimide ester
Boc-L-alanine N-succinimidyl ester, Boc-L-alanine hydroxysuccinimide ester
(S)-2-[[(1,1-Dimethylethoxy)carbonyl]amino]propionic acid 2,5-dioxopyrrolidin-1-yl ester
[(S)-1-[[(2,5-Dioxo-1-pyrrolidinyl)oxy]carbonyl]ethyl]carbamic acid 1,1-dimethylethyl ester
N-(tert-Butoxycarbonyl)alanine 2,5-dioxopyrrolizino
N-(tert-Butoxycarbonyl)-L-alanine 2,5-dioxopyrrolizino
N-(tert-Butyloxycarbonyl)-L-alanine 2,5-dioxopyrrolizino
[EINECS(EC#)]

222-229-7
[Molecular Formula]

C12H18N2O6
[MDL Number]

MFCD00037907
[Molecular Weight]

286.28
[MOL File]

3392-05-0.mol
Chemical PropertiesBack Directory
[Melting point ]

161-163 °C
[alpha ]

-52 º (c=2.5% in dioxane)
[density ]

1.27±0.1 g/cm3(Predicted)
[storage temp. ]

−20°C
[solubility ]

Soluble in water or 1% acetic acid
[form ]

Powder
[pka]

10.81±0.46(Predicted)
[optical activity]

[α]20/D 52±3.5°, c = 2.5% in dioxane
[Sensitive ]

Moisture Sensitive
[BRN ]

3560476
[CAS DataBase Reference]

3392-05-0(CAS DataBase Reference)
Safety DataBack Directory
[Safety Statements ]

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[F ]

3-10-21
[HS Code ]

29224999
Hazard InformationBack Directory
[Chemical Properties]

White powder
[Uses]

Reactant involved in synthesis of:
  • Muramyldipeptide analogs via solid-phase synthesis
  • Microcin C analogs for use as antibacterials
  • Lipid I and nucleoside diphosphate peptide derivatives via N-methylimidazolium chloride catalyzed coupling
  • N-Protected dipeptide acids
  • Free and peptide-bound glycated amino acids for studies of interactions with human Caco-2 interstinal epithelial cell apical membrane transport proteins
  • 7-Substituted camptothecin conjugates with RGD-peptides as avβ3 integrin ligands
[reaction suitability]

reaction type: Boc solid-phase peptide synthesis
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

3392-05-0(sigmaaldrich)
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