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Key Documents

446033

Sigma-Aldrich

Fmoc-2-Abz-OH

97%

Synonym(s):

2-(Fmoc-amino)benzoic acid, N-Fmoc-anthranilic acid

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About This Item

Empirical Formula (Hill Notation):
C22H17NO4
CAS Number:
Molecular Weight:
359.37
Beilstein:
7659726
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

mp

216-218 °C (lit.)

application(s)

peptide synthesis

functional group

Fmoc

SMILES string

OC(=O)c1ccccc1NC(=O)OCC2c3ccccc3-c4ccccc24

InChI

1S/C22H17NO4/c24-21(25)18-11-5-6-12-20(18)23-22(26)27-13-19-16-9-3-1-7-14(16)15-8-2-4-10-17(15)19/h1-12,19H,13H2,(H,23,26)(H,24,25)

InChI key

CNAVPEPPAVHHKN-UHFFFAOYSA-N

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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

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Mihai Ciustea et al.
Journal of medicinal chemistry, 51(20), 6563-6570 (2008-09-24)
Variola virus, the causative agent of smallpox, is a potential bioweapon. The development of new antiviral compounds for smallpox prophylaxis and treatment is critical, especially because the virus can acquire resistance to the drugs that are currently available. We have

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