213881-38-0

Basic information

• Product Name: 2-methyl-8-quinolinyl benzenesulfonate
• Synonyms: 2-methyl-8-quinolinyl benzenesulfonate
• CAS NO: 213881-38-0
• Molecular Formula: C₁₆H₁₃NO₃S
• Molecular Weight: 299.34432
• Mol File: 213881-38-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-methyl-8-quinolinyl benzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methyl-8-quinolinyl benzenesulfonate(213881-38-0)
• EPA Substance Registry System: 2-methyl-8-quinolinyl benzenesulfonate(213881-38-0)

Safety Data

• Hazardous Substances Data: 213881-38-0(Hazardous Substances Data)

Upstream product

• 826-81-3 2-methyl-8-quinolinol 
• 98-09-9 benzenesulfonyl chloride 

Downstream Products

• 826-81-3 2-methyl-8-quinolinol 
• 3198-32-1 benzenesulfonate 
• 213881-33-5 ((R,R)-2S)-N-(2-hydroxy-1-methyl-2-phenylethyl)-N-methyl-2-amino-3-[2-(8-benzenesulfonyloxy)quinolinyl]propionamide 
• 213881-32-4 8-benzenesulfonyloxy-2-bromomethylquinoline 

Relevant articles and documents

Targeting DNA binding for NF-κB as an anticancer approach in hepatocellular carcinoma

Quinoline core has been shown to possess a promising role in the development of anticancer agents. However, the correlation between its broad spectrum of bioactivity and the underlying mechanism of actions is poorly understood. The present study, with the

COMPOUND, COLOR MATERIAL COMPOSITION CONTAINING THE SAME, AND RESIN COMPOSITION CONTAINING THE SAME

PROBLEM TO BE SOLVED: To provide a novel compound, a color material composition containing the same and a resin composition containing the same that improve the color purity, luminance and contrast ratio in color filter production employing a pigment dispersion method using pigments. SOLUTION: The invention provides a compound represented by the chemical formula 1, a color material composition containing the same, and a resin composition containing the same. (Y is a direct bond or CQ1Q2; R1-R14, Q1 and Q2 are each independently H, D, or a halogen group, nitrile group, nitro group, hydroxy group, carbonyl group, ester group, imide group, amide group, carboxy group (-COOH), or -OC(=O)R'''; and the like.) SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2017,JPOandINPIT

Evaluation of some quinoline-based hydrazone derivatives as insecticidal agents

In continuation of our program aimed at the discovery and development of efficient insecticidal agents, a series of quinoline-based hydrazone derivatives were synthesized and evaluated as insecticidal agents against three-day-old larvae of Spodoptera litura (Noctuidae: Lepidoptera), a polyphagous insect pest of many important crops, in vivo at 1 mg mL1. In particular, compounds 3c, 3e, 4g, 4h, and 6f showed potent insecticidal activity with 7 day mortality rates greater than 93%, and were comparable to that of the positive control toosendanin.

Photochemical cleavage reactions of 8-quinolinyl sulfonates in aqueous solution

Photochemical cleavage reactions of 8-quinolinyl benzenesulfonate derivatives and related sulfonates in aqueous solutions are reported. The 8-quinolinyl benzenesulfonates undergo photolysis upon photoirradiation at 300-330 nm to give the corresponding 8-quinolinols and benzenesulfonic acids with the production of only negligible amounts of byproducts. The effects of substituent groups of the 8-quinolinyl moiety and the benzene ring on the photolysis reactions were examined. Based on steady-state mechanistic studies using a triplet sensitizer, a triplet quencher, and electron donors, it was suggested that the photolysis proceeds mainly via the homolytic cleavage of S-O bonds in the excited triplet state.