1160257-16-8

Basic information

• Product Name: 6-ethyl-2-(5-methyl-2-thienyl)quinoline-4-carbonyl chloride
• Synonyms: 6-ethyl-2-(5-methyl-2-thienyl)quinoline-4-carbonyl chloride;4-quinolinecarbonyl chloride, 6-ethyl-2-(5-methyl-2-thieny
• CAS NO: 1160257-16-8
• Molecular Formula: C17H14ClNOS
• Molecular Weight: 315.81716
• Mol File: 1160257-16-8.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 6-ethyl-2-(5-methyl-2-thienyl)quinoline-4-carbonyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 6-ethyl-2-(5-methyl-2-thienyl)quinoline-4-carbonyl chloride(1160257-16-8)
• EPA Substance Registry System: 6-ethyl-2-(5-methyl-2-thienyl)quinoline-4-carbonyl chloride(1160257-16-8)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 1160257-16-8(Hazardous Substances Data)

Usage

Main Properties

1. Quinoline Ring: Contains a quinoline ring as its core structure.
2. Carbonyl Chloride Functional Group: Features a carbonyl chloride functional group (COCl) attached to the quinoline ring.
3. Substituent: Possesses a 5-methyl-2-thienyl substituent attached to the quinoline ring.
4. Reactivity: Exhibits reactivity due to the presence of a reactive carbon atom bonded to both a carbonyl group and a chlorine atom.
5. Usage: Primarily employed in organic chemistry as a reagent for acylating alcohols, amines, and other nucleophiles.
6. Synthetic Utility: Utilized in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals.

Specific Content

1. Derivative of Quinoline: Derived from the organic compound quinoline.
2. Carbonyl Chloride Derivative: Characterized as a carbonyl chloride derivative, indicating its reactive nature.
3. Intermediate Molecule: Serves as an essential intermediate in the production of diverse organic molecules.
4. Applications: Widely used in organic synthesis for preparing pharmaceuticals, agrochemicals, and other organic compounds.