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47307

Sigma-Aldrich

Fmoc-4-Abz-OH

≥96.0% (TLC)

Synonym(s):

4-(Fmoc-amino)benzoic acid

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About This Item

Empirical Formula (Hill Notation):
C22H17NO4
CAS Number:
185116-43-2
Molecular Weight:
359.37
Beilstein/REAXYS Number:
7722986
MDL number:
MFCD00144888
UNSPSC Code:
12352209
PubChem Substance ID:
57650914
NACRES:
NA.26

assay

≥96.0% (TLC)

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

OC(=O)c1ccc(NC(=O)OCC2c3ccccc3-c4ccccc24)cc1

InChI

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

InChI key

VGSYYBSAOANSLR-UHFFFAOYSA-N

Related Categories

Storage Class

11 - 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)

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Chung-Li Ho et al.
Journal of biomedicine & biotechnology, 2011, 101497-101497 (2011-06-11)
Molecular imaging with promise of personalized medicine can provide patient-specific information noninvasively, thus enabling treatment to be tailored to the specific biological attributes of both the disease and the patient. This study was to investigate the characterization of DO3A-CH(2)CO-G-4-aminobenzoyl-Q-W-A-V-G-H-L-M-NH(2) (AMBA)

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