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

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

Uses

Used in Pharmaceutical Synthesis:
2-Quinolinecarboxylic acid, 5,6,7,8-tetrahydro-8-oxois used as a key intermediate in the synthesis of various pharmaceuticals for its potential pharmacological properties. Its anti-inflammatory and antioxidant effects make it a promising candidate for the development of new drugs targeting inflammation and oxidative stress-related conditions.
Used in Organic Chemistry:
2-Quinolinecarboxylic acid, 5,6,7,8-tetrahydro-8-oxois utilized as a building block in organic chemistry for the synthesis of a wide range of organic compounds. Its unique structure allows for various chemical reactions, enabling the creation of diverse molecules with potential applications in different fields.
Used in Agrochemical Production:
2-Quinolinecarboxylic acid, 5,6,7,8-tetrahydro-8-oxois used as a starting material in the synthesis of certain herbicides and pesticides. Its incorporation into these products contributes to the development of effective and targeted agrochemicals for crop protection and weed management.

Upstream product

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

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.

Role of pyridine hydrogen-bonding sites in recognition of basic amino acid side chains

A series of three, new artificial receptors for guanidinium and ammonium guests has been synthesized. All three receptors have highly preorganized clefts bearing two carboxylate groups. They differ in the number of nitrogen atoms contained in their clefts

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.

A small-molecule guanidinium receptor: The arginine cork

A highly preorganized, artificial receptor for guanidinium cations binds arginine with high affinity in polar solvents, even in water! The X-ray crystal structure of its bis(N-ethylguanidinium) complex shows the formation of hydrogen bonds between the rec