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N-(N-Benzyloxycarbonyloxy)succinimide
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N-(N-Benzyloxycarbonyloxy)succinimide

CAS: 13139-17-8

Ref. TR-B286275

25g
112.00 €
Estimated delivery in United States, on Thursday 20 Jun 2024

Product Information

Name:
N-(N-Benzyloxycarbonyloxy)succinimide
Controlled Product
Synonyms:
  • 1-[[(Benzyloxy)carbonyl]oxy]-2,5-pyrrolidinedione
  • 1-[[(Phenylmethoxy)carbonyl]oxy]-2,5-pyrrolidinedione
  • 1-[[[(Phenylmethyl)oxy]carbonyl]oxy]-2,5-pyrrolidinedione
  • Benzyl 2,5-dioxopyrrolid-1-yl Carbonate
  • Benzyl 2,5-dioxopyrrolidin-1-yl Carbonate
  • Benzyl N-succinimidyl Carbonate
  • Benzyl Succinimidyl Carbonate
  • Benzyloxycarbonyloxysuccinimide
  • Cbz-OSu
  • N-(Benzyloxycarbonyloxy)succinimide
  • See more synonyms
  • 1-{[(Benzyloxy)Carbonyl]Oxy}Pyrrolidine-2,5-Dione
  • 2,5-Pyrrolidinedione, 1-[[(phenylmethoxy)carbonyl]oxy]-
  • Benzyl 2,5-dioxopyrrolid-1-yl carbonate
  • Benzyl 2,5-dioxopyrrolidin-1-yl carbonate
  • Benzyl N-succinimidyl carbonate
  • Benzyl succinimidyl carbonate
  • Carbonic acid, 2,5-dioxo-1-pyrrolidinyl phenylmethyl ester
  • Carbonic acid, monobenzyl ester, succinimido deriv.
  • Cbz-Osu
  • O-Benzyloxycarbonyl-N-hydroxysuccinimide
  • Succinimide, N-(carboxyoxy)-, benzyl ester
  • Z-ONSu
  • Z-OSu
Description:

Applications N-(N-Benzyloxycarbonyloxy)succinimide is a reagent used in the preparation of peptide thioacids view peptide precursors. Also used in the preparation of aminoglycoside derivatives for the function of topoisomerase, both human and bacterial inhibition.
References Pira, S. et al.: Org. Lett., 15, 5346 (2013); Fenner, A. et al.: Tetrahedron, 54, 3298 (2013);

Brand:
TRC
Long term storage:
Notes:

Chemical properties

Molecular weight:
249.22
Formula:
C12H11NO5
Color/Form:
White Solid
InChI:
InChI=1S/C12H11NO5/c14-10-6-7-11(15)13(10)18-12(16)17-8-9-4-2-1-3-5-9/h1-5H,6-8H2
InChI key:
InChIKey=MJSHDCCLFGOEIK-UHFFFAOYSA-N
SMILES:
O=C(OCc1ccccc1)ON1C(=O)CCC1=O
MDL:
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EINECS:
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HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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