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84906-81-0,MFCD02179738
Catalog No.:AA003HDC
84906-81-0 | 2-Hydroxyquinoline-4-carboxylic acid
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1g
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$149.00
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5g
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10g
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25g
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  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003HDC
Chemical Name:
2-Hydroxyquinoline-4-carboxylic acid
CAS Number:
84906-81-0
Molecular Formula:
C10H7NO3
Molecular Weight:
189.1675
MDL Number:
MFCD02179738
IUPAC Name:
2-oxo-1H-quinoline-4-carboxylic acid
InChI:
InChI=1S/C10H7NO3/c12-9-5-7(10(13)14)6-3-1-2-4-8(6)11-9/h1-5H,(H,11,12)(H,13,14)
InChI Key:
MFSHNFBQNVGXJX-UHFFFAOYSA-N
SMILES:
Oc1nc2ccccc2c(c1)C(=O)O
EC Number:
239-827-9
UNII:
Z1Q2K479UQ
NSC Number:
3564
Properties
Computed Properties
 
Complexity:
309  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
189.043g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
189.17g/mol
Monoisotopic Mass:
189.043g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
66.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.6  

Synonyms
 
2-Hydroxyquinoline-4-carboxylic acid 
15733-89-8 
2-Hydroxy-quinoline-4-carboxylic acid 
4CH-023579 
AK00739687 
AM20070290 
BB 0221218 
BB 0221230 
EU-0001998 
FT-0612590 
FT-0612638 
FT-0648864 
H2474 
1,2-Dihydro-2-oxoquinoline-4-carboxylic acid 
1,2-dihydro-2-oxo-4-Quinolinecarboxylic acid 
2-Oxo-1,2-dihydro-4-quinolinecarboxylic acid 
EN300-00825 
MFCD00023942 (98%) 
2-oxidanylidene-1H-quinoline-4-carboxylic acid 
2-Oxo-1,2-dihydro-quinoline-4-carboxylic acid 
33H898 
A-2594 
C16715 
M-7537 
2-hydroxy-4-quinolinecarboxylic acid 
2-Oxo-1,2-dihydro-4-quinolinecarboxylic acid # 
733O898 
A809841 
SR-01000403999 
SR-01000597059 
SR-01000403999-1 
SR-01000597059-1 
SR-01000597059-2 
W-108003 
F0346-1608 
UNII-Z1Q2K479UQ 
2-Oxo-1,2-dihydroquinoline-4-carboxylic acid, AldrichCPR 
InChI=1/C10H7NO3/c12-9-5-7(10(13)14)6-3-1-2-4-8(6)11-9/h1-5H,(H,11,12)(H,13,14) 
C10H7NO3 
C10-H7-N-O3 
CID85076 
AR-1E2792 
2-oxo-1,2-dihydroquinoline-4-carboxylate 
C3237 
H1016 
2-Hydroxyquinoline-4-carboxylic acid, 98% 1g 
2-oxo-1H-quinoline-4-carboxylic acid 
4-Quinolinecarboxylic acid, 2-hydroxy- (9CI) 
2-Hydroxyquinoline-4-carboxylic acid, 98% - 1G 1g 
1034-01-1 
851547-34-7 
90937-07-8 
EINECS 239-827-9 
MFCD00023942 
4-Quinolinecarboxylic acid, 2-hydroxy- 
2-HYDROXYQUINOLINE-4-CARBOXYLICACID 
AI3-61768 
84906-81-0 
Z1Q2K479UQ 
CHEBI:52045 
MFSHNFBQNVGXJX-UHFFFAOYSA-N 
H2-hqc 
PubChem6106 
Cinchocaine Impurity B 
PubChem15647 
ACMC-209dfz 
Enamine_001230 
AC1L38RC 
2-oxo-1,2-dihydroquinoline-4-carboxylic acid 
AC1Q5T5W 
Cambridge id 5133898 
Oprea1_034107 
SCHEMBL662652 
AC1Q72O8 
IFLab1_001493 
SCHEMBL8729784 
Jsp003112 
CHEMBL2048387 
CTK3E7885 
2-Hydroxycinchoninic acid 
MFSHNFBQNVGXJX-UHFFFAOYSA- 
2-oxo-4-quinolinecarboxylic acid 
DTXSID40166250 
NSC3564 
HMS1397H20 
HMS1416D19 
AC1Q7338 
ACT06764 
ALBB-010502 
BCP28536 
2-Hydroxy-4-quinolincarboxylic acid 
CCG-1662 
KS-00000G3G 
KS-000048SZ 
NSC-3564 
ZINC8579968 
ANW-21693 
BBL008901 
BBL011718 
CH-188 
HTS027683 
4-Carboxycarbostyril 
SBB028512 
STK078430 
STK709494 
IFLAB-BB F1918-0080 
2-Hydroxyquinolinecarboxylic acid-(4) 
4-Quinolinecarboxylicacid, 2-hydroxy- 
AKOS000104068 
AKOS000266346 
2(1H)-Oxoquinoline-4-carboxylic acid 
AC-1861 
Cinchoninic acid, 2-hydroxy- 
AN-1255 
CCG-104483 
CM14326 
CS-W015953 
LS20669 
MCULE-7215935191 
RP24891 
SDCCGMLS-0065426.P001 
TRA0047426 
VQ10122 
4-Quinolinecarboxylic acid, 1,2-dihydro-2-oxo- 
NCGC00246893-01 
AC-23085 
AJ-71330 
AK-25000 
AS-12503 
BC209181 
BR-25000 
LS-53794 
SC-04165 
SC-16757 
2-oxocinchoninic acid 
SC-73494 
ST086513 
SY020050 
Quinoline-4-carboxylic acid, 2(1H)-oxo- 
2-Hydroxyquinoline-4-carboxylic acid, 97% 
AB0012040 
AB0066390 
DB-012013 
ST2410047 
TR-050394 
Literature

Title: Construction and functionalization of fused pyridine ring leading to novel compounds as potential antitubercular agents.

Journal: Bioorganic & medicinal chemistry letters 20120715

Title: Extracts and constituents of Rubus chingii with 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radical scavenging activity.

Journal: International journal of molecular sciences 20110101

Title: Tetra-aqua-bis(2-oxo-1,2-dihydro-quinoline-4-carboxyl-ato-κO)nickel(II).

Journal: Acta crystallographica. Section E, Structure reports online 20080201

Title: The Elbs and Boyland-Sims peroxydisulfate oxidations.

Journal: Beilstein journal of organic chemistry 20060101

Title: Parallel liquid-phase synthesis of N-substituted 6-aminosulfonyl-2-oxo-1,2-dihydroquinoline-4-carboxamide and 6-aminosulfonylquinoline-4-carboxamide derivatives.

Journal: Journal of combinatorial chemistry 20050101

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