196479
2-Phenyl-4-quinolinecarboxylic acid
99%
Synonym(s):
2-Phenylcinchoninic acid, Cinchophen
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About This Item
Empirical Formula (Hill Notation):
C16H11NO2
CAS Number:
Molecular Weight:
249.26
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
powder
mp
214-215 °C (lit.)
solubility
alcohol: soluble 1g in 120ml(lit.)
chloroform: soluble 1g in 400ml(lit.)
diethyl ether: soluble 1g in 100ml(lit.)
water: insoluble(lit.)
SMILES string
OC(=O)c1cc(nc2ccccc12)-c3ccccc3
InChI
1S/C16H11NO2/c18-16(19)13-10-15(11-6-2-1-3-7-11)17-14-9-5-4-8-12(13)14/h1-10H,(H,18,19)
InChI key
YTRMTPPVNRALON-UHFFFAOYSA-N
Related Categories
General description
2-Phenyl-4-quinolinecarboxylic acid on reaction with 5-aryl-2,3-dihydro-2,3-furandiones yields β-aroylpyruvoyl hydrazide of 2-phenyl-4-quinolinecarboxylic acid.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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A Takahashi et al.
Journal of gastroenterology, 31(2), 153-160 (1996-04-01)
The contribution of granulocytes and their byproducts to acute gastric mucosal lesion (AGML) is unclear. Our previous study showed that granulocytes produced O2- in the gastric mucosa of rats treated with 300 mg/kg of cinchophen (cinchophen ulcer, CU) and in
Structure-action relationship among drugs acting on connective tissues (anti-rheumatic agents).
M W WHITEHOUSE
Nature, 194, 984-985 (1962-06-09)
ROLE OF DRUGS IN PRODUCTION OF GASTRODUODENAL ULCER.
J L ROTH
JAMA, 187, 419-422 (1964-02-08)
ANTI-INFLAMMATORY ACTIVITY ON NONSTEROIDAL AGENTS IN A RAT GRANULOMA ASSAY.
R I DORFMAN et al.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.), 119, 859-862 (1965-07-01)
[ON THE TREATMENT OF GOUT. LESSONS ON THE COURSE OF THERAPY. II. PHARMACOLOGICAL TREATMENT].
G IZAR
Minerva medica, 55, 2571-2580 (1964-09-01)
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