238755-39-0

Basic information

• Product Name: 2-Quinolinecarboxylic acid, 5,6,7,8-tetrahydro-8-oxo-
• Synonyms: 2-Quinolinecarboxylic acid, 5,6,7,8-tetrahydro-8-oxo-;8-Oxo-5,6,7,8-tetrahydroquinoline-2-carboxylic acid
• CAS NO: 238755-39-0
• Molecular Formula: C10H9NO3
• Molecular Weight: 191.18336
• Mol File: 238755-39-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 427.0±45.0 °C(Predicted)
• Appearance: /
• Density: 1.380±0.06 g/cm3(Predicted)
• PKA: 0.74±0.20(Predicted)
• CAS DataBase Reference: 2-Quinolinecarboxylic acid, 5,6,7,8-tetrahydro-8-oxo-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Quinolinecarboxylic acid, 5,6,7,8-tetrahydro-8-oxo-(238755-39-0)
• EPA Substance Registry System: 2-Quinolinecarboxylic acid, 5,6,7,8-tetrahydro-8-oxo-(238755-39-0)

Safety Data

• Hazardous Substances Data: 238755-39-0(Hazardous Substances Data)

Usage

General Description

2-Quinolinecarboxylic acid, 5,6,7,8-tetrahydro-8-oxo- is a chemical compound with the molecular formula C10H9NO3. It is a heterocyclic compound derived from quinoline and carboxylic acid, and its structure includes a tetrahydro-8-oxo- group. 2-Quinolinecarboxylic acid, 5,6,7,8-tetrahydro-8-oxo- has been studied for its potential pharmacological properties, including anti-inflammatory and antioxidant effects. It has also been investigated for its potential use in the synthesis of pharmaceuticals and other organic compounds. Additionally, it is a key starting material in the synthesis of certain herbicides and pesticides.

Upstream product

• 238755-38-9 6,7-dihydro-8(5H)-quinolinone-2-carboxaldehyde 
• 91-63-4 2-methylquinoline 
• 2617-98-3 2-methyl-5,6,7,8-tetrahydroquinoline 

Relevant articles and documents

Bicarbonate receptor compounds

The invention relates to a compound having the general formula I wherein A1 and A2 are selected from the group consisting of carbon (=CH-) and nitrogen (=N-); D1 and D2 are selected from the group consisting of-OH, -SH and -NHR1 groups, wherein R1 is hydrogen, hydrophilic substituent, hydrophobic substituent or linker; X1 and X2 are selected from the group consisting of oxygen (=O), sulphur (=S) and =NR2 group, wherein R2 is hydrogen, hydrophilic substituent, hydrophobic substituent or linker; X3 is selected from the group consisting of oxygen (=O), sulphur (=S), =NR2 group and two singly bonded moieties, wherein both moieties are hydrogen or one moiety is hydrogen and the other moiety is selected from the group of hydrophilic substituent, hydrophobic substituent and linker; and R1-R9 are selected from the group consisting of hydrogen, electron donating substituent, electron accepting substituent, hydrophilic substituent, hydrophobic substituent and linker, or R3 and R4 and/or R6 and R7 form together an aromatic or heteroaromatic, substituted or unsubstituted ring and the remaining moieties R1-R9 are as defined above.

Methods and kits for the detection of arginine compounds

Methods and kits for determine arginine compounds are discussed. The methods and kits of the invention can be used for the diagnosis of arginine compound associated disorders.