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Key Documents

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:
Molecular Weight:
249.26
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

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

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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