328898
9-Fluoreneacetic acid
99%
Synonym(s):
9-Fluorenylacetic acid
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C15H12O2
CAS Number:
Molecular Weight:
224.25
Beilstein/REAXYS Number:
1969039
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
assay
99%
mp
133-135 °C (lit.)
SMILES string
OC(=O)CC1c2ccccc2-c3ccccc13
InChI
1S/C15H12O2/c16-15(17)9-14-12-7-3-1-5-10(12)11-6-2-4-8-13(11)14/h1-8,14H,9H2,(H,16,17)
InChI key
WFSMJMTYIMFHPV-UHFFFAOYSA-N
Gene Information
rat ... Akr1b1(24192)
Looking for similar products? Visit Product Comparison Guide
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)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Y S Lee et al.
Bioorganic & medicinal chemistry, 6(10), 1811-1819 (1998-12-05)
Molecular modeling studies using the CHARMM method have been conducted to study the binding modes of aldose reductase inhibitors at the active site of aldose reductase. The energy minimized structures of aldose reductase with six structurally diverse inhibitors (spirofluorene-9,5'-imidazolidine-2',4'-dione (1)
P E Teal et al.
Regulatory peptides, 72(2-3), 161-167 (1998-07-04)
Amphiphilic pseudopeptide analogs of Phe-Thr-Pro-Arg-Leu-NH2, representing the active C-terminal core pentapeptide of the pyrokinin class of insect neuropeptides, were synthesized by replacement of phenylalanine with hydrocinnamic acid (Hca-Thr-Pro-Arg-Leu-NH2), or addition of 1-pyrenebutyric acid (Pba-Phe-Thr-Pro-Arg-Leu-NH2) or 9-fluoreneacetic acid (Fla-Phe-Thr-Pro-Arg-Leu-NH2). The pseudopeptides
Isaac O Donkor et al.
Journal of medicinal chemistry, 51(14), 4346-4350 (2008-07-19)
A series of peptidyl alpha-ketoacids and alpha-ketoesters was synthesized and studied as mu-calpain inhibitors. Docking studies revealed that the mu-calpain inhibitory activity of the compounds is influenced by hydrogen bonding interactions and the potential for ionic interaction with active site
H M Zhang et al.
Journal of pharmaceutical and biomedical analysis, 10(8), 577-586 (1992-08-01)
Two silica reagents based on a 4-hydroxy-3-nitrobenzoyl backbone were synthesized and characterized with 9-fluorenylmethoxycarbonyl (FMOC) and 9-fluoreneacetyl (FA) tags. These reagents were tested by derivatization of primary and secondary amines. Derivatization conditions such as temperature, time and triethylamine catalyst were
F X Zhou et al.
Journal of chromatography, 619(1), 93-101 (1993-09-08)
A simple, highly sensitive and selective method is described for adamantanamine determination in plasma and urine by high-performance liquid chromatography with fluorescence detection. The method involved a simultaneous extraction and derivatization of biological fluids with a 9-fluoreneacetate (9-FA) solid-phase derivatization
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
