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46916

Sigma-Aldrich

9-Fluorenylmethyl carbamate

≥99.0% (HPLC)

Synonym(s):

Fmoc-amide

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About This Item

Empirical Formula (Hill Notation):
C15H13NO2
CAS Number:
84418-43-9
Molecular Weight:
239.27
Beilstein/REAXYS Number:
4188192
MDL number:
MFCD00237376
UNSPSC Code:
12352005
PubChem Substance ID:
329757263
NACRES:
NA.22

assay

≥99.0% (HPLC)

form

solid

mp

201-204 °C

solubility

dioxane: 15 mg/mL, clear, colorless

application(s)

peptide synthesis

SMILES string

NC(=O)OCC1c2ccccc2-c3ccccc13

InChI

1S/C15H13NO2/c16-15(17)18-9-14-12-7-3-1-5-10(12)11-6-2-4-8-13(11)14/h1-8,14H,9H2,(H2,16,17)

InChI key

ZZOKVYOCRSMTSS-UHFFFAOYSA-N

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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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Choi Yi Li et al.
Chembiochem : a European journal of chemical biology, 20(1), 46-50 (2018-09-19)
Urokinase-type plasminogen activator (uPA) and tissue-type plasminogen activator (tPA) are two serine proteases that contribute to initiating fibrinolysis by activating plasminogen. uPA is also an important tumour-associated protease due to its role in extracellular matrix remodelling. Overexpression of uPA has
Simon J de Veer et al.
The Biochemical journal, 469(2), 243-253 (2015-05-20)
Laskowski inhibitors regulate serine proteases by an intriguing mode of action that involves deceiving the protease into synthesizing a peptide bond. Studies exploring naturally occurring Laskowski inhibitors have uncovered several structural features that convey the inhibitor's resistance to hydrolysis and

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