| Identification | Back Directory | [Name]
BOC-OSU | [CAS]
13139-12-3 | [Synonyms]
BOC-OSU
BOC-ONSU
BOC-OSU PURUM
Boc-OSu >=98.0% (CHN)
LABOTEST-BB LT00645757
T-BUTYL N-SUCCINIMIDO CARBONATE
T-BUTYL N-SUCCINIMIDYL CARBONATE
tert-butyl succinimido carbonate
TERT-BUTYL N-SUCCINIMIDYL CARBONATE
N-(TERT-BUTOXYCARBONYLOXY)SUCCINIMIDE
N-TERT-BUTYLOXYCARBONYLOXY-SUCCINIMIDE
OC-OSU tert-Butyl N-succiniMidyl carbonate
N-(tert-Butoxycarbonyloxy)succiniMide, 98+%
Boc-Osu tert-Butyl N-succinimidyl carbonate
tert-Butyl (2,5-dioxopyrrolidin-1-yl) carbonate
N-(tert-Butoxycarbonyloxy)succinimide (Boc-OSu)
N-(tert-Butoxycarbonyloxy)succinimide≥99% (HPLC)
1-[[(1,1-dimethylethoxy)carbonyl]oxy]-5-pyrrolidinedione
N-(tert-Butoxycarbonyloxy)succinimide, tert-Butyl N-succinimidyl carbonate
Boc-Osu,N-(Tert-Butoxycarbonyloxy)SucciniMide, Tert-Butyl N-SucciniMidyl Carbonate | [EINECS(EC#)]
236-071-1 | [Molecular Formula]
C9H13NO5 | [MDL Number]
MFCD00037903 | [MOL File]
13139-12-3.mol | [Molecular Weight]
215.2 |
| Chemical Properties | Back Directory | [Melting point ]
~95 °C (dec.)
| [Boiling point ]
272.8±23.0 °C(Predicted) | [density ]
1.26±0.1 g/cm3(Predicted) | [storage temp. ]
−20°C
| [solubility ]
sol ether, ethyl acetate, acetone; insol water, petroleum ether. | [form ]
Powder | [color ]
White | [Sensitive ]
Moisture Sensitive | [BRN ]
1536756 | [InChI]
InChI=1S/C9H13NO5/c1-9(2,3)14-8(13)15-10-6(11)4-5-7(10)12/h4-5H2,1-3H3 | [InChIKey]
VTGFSVGZCYYHLO-UHFFFAOYSA-N | [SMILES]
C(ON1C(=O)CCC1=O)(=O)OC(C)(C)C | [CAS DataBase Reference]
13139-12-3 | [EPA Substance Registry System]
2,5-Pyrrolidinedione, 1-[[(1,1-dimethylethoxy)carbonyl]oxy]- (13139-12-3) |
| Hazard Information | Back Directory | [Description]
Boc-OSu is a reagent in peptide synthesis that protects amino acid amine groups as a selective protecting group. It forms a stable carbamate with the amine in the presence of a base, preventing unwanted reactions. This selective protection and deprotection process is key to the stepwise synthesis of peptides. | [Mechanism of action]
Boc-OSu′s mechanism of action involves the formation of a covalent bond with the amine group, effectively blocking its reactivity until the deprotection step is initiated. This reagent is useful in the controlled and efficient synthesis of peptides by providing a means to protect specific functional groups, allowing for the precise manipulation of peptide sequences. |
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