Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

331538

Sigma-Aldrich

9-Fluorenylmethyl 1-benzotriazolyl carbonate

98%

Synonym(s):

Benzotriazol-1-yl 9-fluorenylmethyl carbonate, Fmoc-OBt

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C21H15N3O3
CAS Number:
Molecular Weight:
357.36
Beilstein/REAXYS Number:
5359247
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

assay

98%

form

solid

mp

178 °C (dec.) (lit.)

application(s)

peptide synthesis

storage temp.

2-8°C

SMILES string

O=C(OCC1c2ccccc2-c3ccccc13)On4nnc5ccccc45

InChI

1S/C21H15N3O3/c25-21(27-24-20-12-6-5-11-19(20)22-23-24)26-13-18-16-9-3-1-7-14(16)15-8-2-4-10-17(15)18/h1-12,18H,13H2

InChI key

KNSPZTVPSAKHBN-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

9-Fluorenylmethyl 1-benzotriazolyl carbonate can be used as a protecting agent in the synthesis of:
  • An O-phosphotyrosine analog applicable in the peptide synthesis.[1]
  • Complex glycopeptides.[2]

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Preparation of 4-[bis (tert-butoxy) phosphorylmethyl]-N-(fluoren-9-ylmethoxycarbonyl)-DL-phenylalanine. A hydrolytically stable analogue of O-phosphotyrosine potentially suitable for peptide synthesis
Burke Jr TR, et al.
Synthesis, 1991(11), 1019-1020 (1991)
Efficient synthesis of complex glycopeptides based on unprotected oligosaccharides
Xue J and Guo Z
The Journal of Organic Chemistry, 68(7), 2713-2719 (2003)

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service