F6605
3-Fluorobenzoic acid
97%
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About This Item
Formula condensata:
FC6H4CO2H
Numero CAS:
Peso molecolare:
140.11
Beilstein:
1906920
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Saggio
97%
Punto di fusione
122-124 °C (lit.)
Stringa SMILE
OC(=O)c1cccc(F)c1
InChI
1S/C7H5FO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4H,(H,9,10)
MXNBDFWNYRNIBH-UHFFFAOYSA-N
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Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organi bersaglio
Respiratory system
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 1
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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I clienti hanno visto anche
F G Hidde Boersma et al.
FEMS microbiology letters, 237(2), 355-361 (2004-08-24)
While several microorganisms readily degrade 2- and 4-fluorobenzoates, only a very small number appear to catabolise the 3-fluoro isomer, owing to the accumulation of toxic intermediates. Here we describe the isolation of a bacterium capable of using 3-fluorobenzoate as a
C J Springer et al.
Journal of medicinal chemistry, 37(15), 2361-2370 (1994-07-22)
The synthesis of six novel fluorinated potential prodrugs for antibody-directed enzyme prodrug therapy is described. The [2- and 3-fluoro-4-[bis(2-chloroethyl)amino]benzoyl]-L-glutamic acid (9 and 21), their bis(mesyloxy)ethyl derivatives (7 and 19), and their chloroethyl (mesyloxy)-ethyl derivatives (8 and 20) are bifunctional alkylating
Metabolism of monofluoro- and monochlorobenzoates by a dentrifying bacterium.
B F Taylor et al.
Archives of microbiology, 122(3), 301-306 (1979-09-01)
J B J H van Duuren et al.
Journal of biotechnology, 156(3), 163-172 (2011-09-13)
Pseudomonas putida KT2440-JD1 was derived from P. putida KT2440 after N-methyl-N'-nitro-N-nitrosoguanidine (NTG)-mutagenesis and exposure to 3-fluorobenzoate (3-FB). The mutant was no longer able to grow using benzoate as a sole carbon source, but co-metabolized benzoate to cis, cis-muconate during growth
R Miura
Journal of biochemistry, 105(2), 318-322 (1989-02-01)
The interactions of competitive inhibitors, o-, m-, and p-fluorobenzoates, with porcine kidney D-amino acid oxidase (DAO) were studied by 19F-NMR spectroscopy. The 19F-signals of DAO-bound fluorobenzoates were observed as considerably broadened peaks. The chemical shifts, which are referenced to 20
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