Product Name :
3-Fluoro-4-hydroxybenzoic acid (CAS 350-29-8)
Synonym :
Application :
CAS:
350-29-8
Purity:
Molecular Weight:
156.11
Formula :
C7H5FO3
Physical state:
Solid
solubility :
Shipping Condition :
Store at 4° C
Melting point:
154-158° C (lit.)
SMILES:
OC(=O)C1=CC(F)=C(O)C=C1
References:
:TEAC antioxidant activity of 4-hydroxybenzoates. | Tyrakowska, B., et al. 1999. Free Radic Biol Med. 27: 1427-36. PMID: 10641737Use of Fluorinated Compounds To Detect Aromatic Metabolites from m-Cresol in a Methanogenic Consortium: Evidence for a Demethylation Reaction. | Londry, KL. and Fedorak, PM. 1993. Appl Environ Microbiol. 59: 2229-38. PMID: 16348996Mild and highly flexible enzyme-catalyzed modification of poly(ethersulfone) membranes. | Nady, N., et al. 2011. ACS Appl Mater Interfaces. 3: 801-10. PMID: 21344870Autodisplay of nitrilase from Klebsiella pneumoniae and whole-cell degradation of oxynil herbicides and related compounds. | Detzel, C., et al. 2013. Appl Microbiol Biotechnol. 97: 4887-96. PMID: 22987202A novel pan-negative-gating modulator of KCa2/3 channels, fluoro-di-benzoate, RA-2, inhibits endothelium-derived hyperpolarization-type relaxation in coronary artery and produces bradycardia in vivo. | Oliván-Viguera, A., et al. 2015. Mol Pharmacol. 87: 338-48. PMID: 25468883Protocatechuate 3,4-dioxygenase: implications of ionization effects on binding and dissociation of halohydroxybenzoates and on catalytic turnover. | May, SW. and Phillips, RS. 1979. Biochemistry. 18: 5933-9. PMID: 42436Protocatechuate 3,4-dioxygenase. Mechanistic implications of inhibition by the transition state analog, 2-hydroxyisonicotinic acid N-oxide.1227585-36-5 Molecular Weight | May, SW., et al. 1982. J Biol Chem. 257: 12746-51. PMID: 6813328Purification and properties of 4-hydroxybenzoate 1-hydroxylase (decarboxylating), a novel flavin adenine dinucleotide-dependent monooxygenase from Candida parapsilosis CBS604. | Eppink, MH., et al. 1997. J Bacteriol. 179: 6680-7. PMID: 93529163.0.CO;2-5″ target=”_blank” rel=”nofollow”>Effect of lateral substituents on the mesomorphic properties of side-chain liquid crystalline polysiloxanes containing 4-[(S)-2-methyl-1-butoxy]phenyl 4-(alkenyloxy)benzoate side groups | Chain-Shu Hsu,Pei-Hwei Chu,Huey-Ling Chang,Tong-Hong Hsieh.1559067-56-9 SMILES 1997.PMID:33565366 Journal of Polymer Science Part A: Polymer Chemistry. 35: 2793-2800.Biaxial smectic A phase in homologous series of compounds composed of highly polar unsymmetrically substituted bent-core molecules | B. K. Sadashiva,*a R. Amaranatha Reddy,a R. Pratibhaa and N. V. Madhusudanaa . 2002. J. Mater. Chem. 12: 943-950.Synthesis of Fluorosubstituted Three Ring Esters and Their Dielectric Properties | Dorota Ziobro , Jerzy Dziaduszek , Marek Filipowicz , Roman Dąbrowski , Joanna Czub & Stanisław Urban. 2009. Molecular Crystals and Liquid Crystals. 502: 258-271.Direct transition from a nematic phase to a polar biaxial smectic A phase in a homologous series of unsymmetrically substituted bent-core compounds | R. Amaranatha Reddya and B. K. Sadashiva*a . 2014. J. Mater. Chem. 14: 310-319.Stereoselective radiosynthesis of l- and d-3-[18F]fluoro- alpha -methyltyrosine | Johnny Castillo Meleán, Sven Humpert, Johannes Ermert, Heinz H. Coenen. 2015. Journal of Fluorine Chemistry. 178: 202-207.