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Merck
CN

192961

4-Hydroxy-7-trifluoromethyl-3-quinolinecarboxylic acid

technical grade, 85%

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About This Item

Empirical Formula (Hill Notation):
C11H6F3NO3
CAS Number:
574-92-5
Molecular Weight:
257.17
NACRES:
NA.22
PubChem Substance ID:
24851573
UNSPSC Code:
12352100
EC Number:
209-377-8
MDL number:
MFCD00006771

Key Documents

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Product Name

4-Hydroxy-7-trifluoromethyl-3-quinolinecarboxylic acid, technical grade, 85%

InChI key

BIRIVPOTERXIOW-UHFFFAOYSA-N

InChI

1S/C11H6F3NO3/c12-11(13,14)5-1-2-6-8(3-5)15-4-7(9(6)16)10(17)18/h1-4H,(H,15,16)(H,17,18)

SMILES string

OC(=O)c1cnc2cc(ccc2c1O)C(F)(F)F

grade

technical grade

assay

85%

mp

259-260 °C (dec.) (lit.)

functional group

carboxylic acid
fluoro

Gene Information

human ... CSNK2A1(1457)

Application

4-Hydroxy-7-trifluoromethyl-3-quinolinecarboxylic acid was used in the preparation of (4-hydroxy-7-trifluoromethylquinolin-3-yl)formaldehyde.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKBD9483V
MKBD9483
MKBD4540
MKBD3813
MKBD3812

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P B Koneru et al.
Pharmaceutical research, 10(4), 515-520 (1993-04-01)
A series of eight new N-hydroxy-N'-aminoguanidine (HAG) Schiff bases [ArCH = NNHC(= NH)NHOH.tosylate] was synthesized as potential antitumor agents through the inhibition of the enzyme ribonucleotide reductase (EC 1.17.4.1). Five of the HAG derivatives (LK02 through LK06) were designed to

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