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:
Molecular Weight:
257.17
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
grade
technical grade
Assay
85%
mp
259-260 °C (dec.) (lit.)
functional group
carboxylic acid
fluoro
SMILES string
OC(=O)c1cnc2cc(ccc2c1O)C(F)(F)F
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)
InChI key
BIRIVPOTERXIOW-UHFFFAOYSA-N
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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
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
Regulatory Information
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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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