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227781

Sigma-Aldrich

N-(Benzyloxycarbonyloxy)succinimide

98%, for peptide synthesis

Synonym(s):

Benzyl N-succinimidyl carbonate, Z-OSu

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About This Item

Empirical Formula (Hill Notation):
C12H11NO5
CAS Number:
Molecular Weight:
249.22
Beilstein:
1387927
EC Number:
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

product name

N-(Benzyloxycarbonyloxy)succinimide, 98%

Assay

98%

mp

80-82 °C (lit.)

application(s)

peptide synthesis

SMILES string

O=C(OCc1ccccc1)ON2C(=O)CCC2=O

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

MJSHDCCLFGOEIK-UHFFFAOYSA-N

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Application

N-(Benzyloxycarbonyloxy)succinimide (Cbz-OSu) is a common reagent for the carboxybenzyl protection of amines. This reaction is one of the key synthetic steps in the synthesis of:
  • Enantiomers of cyclic methionine analogs viz, (R)-and (S)-3-aminotetrahydrothiophene- 3-carboxylic acid.
  • 1′-H-Spiro-(indoline-3,4′-piperidine) and its derivatives.
  • Total synthesis of (-)-diazonamide A. and (-)-sanglifehrin A.

Cbz-OSu is widely employed to protect amino acid residues in peptide synthesis. It can also be used in N-trans diprotection of cyclen regioselectively.
Reagent for the selective introduction of the Z-amino protection in amino acids; and in aminoglycoside antibiotics.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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A convergent three-component total synthesis of the powerful immunosuppressant (−)-sanglifehrin A.
Paquette L A, et al.
Journal of the American Chemical Society, 124(16), 4257-4270 (2002)
Pd/C (en)-Catalyzed chemoselective hydrogenation with retention of the N-Cbz protective group and its scope and limitations.
Hattori K, et al.
Tetrahedron, 56(43), 8433-8441 (2000)
Total synthesis of nominal Diazonamides?Part 1: convergent preparation of the structure proposed for (−)?Diazonamide A.
Li J, et al.
Angewandte Chemie (International Edition in English), 40(24), 4765-4769 (2001)
A general asymmetric synthesis of syn-and anti-β-substituted cysteine and serine derivatives.
Xiong C, et al.
The Journal of Organic Chemistry, 67(10), 3514-3517 (2002)
Reconstitution of peptidoglycan cross-linking leads to improved fluorescent probes of cell wall synthesis.
Lebar M D, et al.
Journal of the American Chemical Society, 136(31), 10874-10877 (2014)

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