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192961

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

Name: 4-Hydroxy-7-trifluoromethyl-3-quinolinecarboxylic acid
Brand: ALDRICH

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

Assay:

85%

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Properties

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)

Description

Application

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

pictograms

GHS07

signalword

Warning

hcodes

H302,H315,H319,H335

pcodes

P261 - P264 - P270 - P301 + P312 - P302 + P352 - P305 + P351 + P338

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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Synthesis and testing of new antileukemic Schiff bases of N-hydroxy-N'-aminoguanidine against CCRF-CEM/0 human leukemia cells in vitro and synergism studies with cytarabine (Ara-C).

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

Global Trade Item Number

SKU	GTIN
192961-10G	04061833313183