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线性分子式:
FC6H3-2-(OH)CO2H
化学文摘社编号:
分子量:
156.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-455-3
Beilstein/REAXYS Number:
2209120
MDL number:
Assay:
97%
Form:
powder
InChI key
JWPRICQKUNODPZ-UHFFFAOYSA-N
InChI
1S/C7H5FO3/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,9H,(H,10,11)
SMILES string
OC(=O)c1cc(F)ccc1O
assay
97%
form
powder
mp
177-179 °C (lit.)
functional group
carboxylic acid, fluoro
Quality Level
Application
5-Fluorosalicylic acid was used as internal standard in the quantification of salicylic acid.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Terézia Szabó-Plánka et al.
Journal of inorganic biochemistry, 102(1), 101-109 (2007-08-28)
The copper(II)-5-fluorosalicylic acid system was investigated in water and 50 v/v% water-methanol mixture by pH potentiometry combined with UV-vis spectrophotometry, and by the two-dimensional ESR simulation method, respectively. The data revealed that the stable paramagnetic mono- and bis(salicylato) copper(II) complexes
Terézia Szabó-Plánka et al.
Journal of inorganic biochemistry, 105(1), 75-83 (2010-12-08)
The complexation of 3-, 4-, and 6-fluorosalicylic acids (HL) with copper(II) was investigated in aqueous solution by pH-potentiometry combined with UV-visible spectrophotometry, and in 50 v/v % water-methanol mixture by the two-dimensional ESR simulation method. Both methods showed the formation
Daiki Asakawa et al.
Journal of the American Society for Mass Spectrometry, 22(7), 1224-1233 (2011-09-29)
The use of 5-formylsalicylic acid (5-FSA) and 5-nitrosalicylic acid (5-NSA) as novel matrices for in-source decay (ISD) of peptides in matrix-assisted laser desorption/ionization (MALDI) is described. The use of 5-FSA and 5-NSA generated a- and x-series ions accompanied by oxidized
T K Christopoulos et al.
Analytical chemistry, 64(4), 342-346 (1992-02-15)
We report an ultrasensitive, enzymatically amplified, time-resolved fluorescence immunoassay with a terbium chelate as the detectable moiety. In this immunoassay, the primary label is the enzyme alkaline phosphatase (ALP). ALP cleaves phosphate out of a fluorogenic substrate, 5-fluorosalicyl phosphate, to
Suja Shrestha et al.
Bioorganic & medicinal chemistry, 15(20), 6535-6548 (2007-08-19)
A series of compounds containing one or two salicylic acid moieties were synthesized, and their efficacy to inhibit the phosphohydrolase activity of PTP1B examined. Some of the methylenedisalicylic acid derivatives were potent inhibitors of PTP1B. Of those derivatives, 3c exhibited
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