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8-Quinolinecarboxylic acid, 1,2,3,4-tetrahydro-6-nitro-, is a chemical compound with the molecular formula C10H10N2O4. It is a derivative of quinoline, a heterocyclic aromatic compound with a benzene ring fused to a pyridine ring. The compound is characterized by the presence of a nitro group (-NO2) at the 6-position and a carboxylic acid (-COOH) group at the 8-position. It is a yellow crystalline solid and is soluble in organic solvents such as ethanol and methanol. 8-QUINOLINECARBOXYLIC ACID, 1,2,3,4-TETRAHYDRO-6-NITRO- has potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical structure and properties.

123296-82-2

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123296-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123296-82-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,2,9 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 123296-82:
(8*1)+(7*2)+(6*3)+(5*2)+(4*9)+(3*6)+(2*8)+(1*2)=122
122 % 10 = 2
So 123296-82-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O4/c13-10(14)8-5-7(12(15)16)4-6-2-1-3-11-9(6)8/h4-5,11H,1-3H2,(H,13,14)

123296-82-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-nitro-1,2,3,4-tetrahydroquinoline-8-carboxylic acid

1.2 Other means of identification

Product number -
Other names 8-QUINOLINECARBOXYLIC ACID, 1,2,3,4-TETRAHYDRO-6-NITRO-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:123296-82-2 SDS

123296-82-2Relevant academic research and scientific papers

Synthesis and antirheumatic activity of novel tetrahydroquinoline-8-carboxylic acid derivatives

Kohno, Yasushi,Awano, Katsuya,Miyashita, Mitsutomo,Fujimori, Shizuyoshi,Kuriyama, Kazuhiko,Sakoe, Yasuhiko,Kudoh, Shinji,Saito, Koji,Kojima, Eisuke

, p. 1515 - 1518 (1997)

A study of the modification of N-alkylanthranilic acids to develop novel DMARDs is detailed. 1,2,3,4-Tetrahydroquinoline-8-carboxylic acid derivatives were found to exhibit a therapeutic effect on adjuvant arthritis and a suppressive effect on bone destruction.

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