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196479

Sigma-Aldrich

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:
132-60-5
Molecular Weight:
249.26
EC Number:
205-067-1
MDL number:
MFCD00006750
UNSPSC Code:
12352100
PubChem Substance ID:
24851762
NACRES:
NA.22

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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Certificates of Analysis (COA)

Lot/Batch Number
STBJ1469
STBD8630V
STBD0089V
STBC9455V
S73837

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[Atophan intoxication].
W ROSE
Archiv fur Toxikologie, 19, 158-163 (1961-01-01)
The role of HCI and pepsin in the mechanism of cinchophen ulcer.
K J HARTIALA et al.
Annales medicinae experimentalis et biologiae Fenniae, 41, 9-14 (1963-01-01)
[THERAPY OF GOUTY ARTHROPATHY].
V MECCOLI
La Clinica terapeutica, 27, 517-523 (1963-12-15)
Structure-action relationship among drugs acting on connective tissues (anti-rheumatic agents).
M W WHITEHOUSE
Nature, 194, 984-985 (1962-06-09)
[GASTRIC PEPSIN RESPONSE TO ACTH RELEASE AND PEPTIC ULCER].
K ISHIHARA
Rinsho geka. Journal of clinical surgery, 19, 161-166 (1964-02-01)
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