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3,4-dichloro-2-(trichloromethyl)quinoline is a quinoline derivative with the molecular formula C10H5Cl5N. It features two chloro substituents at the 3 and 4 positions and a trichloromethyl group attached to the 2 position of the quinoline ring. This white solid is sparingly soluble in water but soluble in organic solvents.

79325-33-0

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79325-33-0 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
3,4-dichloro-2-(trichloromethyl)quinoline is used as a chemical intermediate for the synthesis of pharmaceuticals and agrochemicals. Its unique chemical structure and reactivity make it a valuable component in the development of various medicinal and agricultural products.
Used in Research:
In research settings, 3,4-dichloro-2-(trichloromethyl)quinoline serves as a building block for the preparation of novel organic compounds. Its distinct properties allow scientists to explore new avenues in organic chemistry and potentially discover innovative applications.
Safety Precautions:
Due to its potential as a skin and eye irritant, 3,4-dichloro-2-(trichloromethyl)quinoline should be handled with care in a controlled laboratory environment. Proper safety measures and precautions are essential to minimize hazards during its use.

Check Digit Verification of cas no

The CAS Registry Mumber 79325-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,2 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79325-33:
(7*7)+(6*9)+(5*3)+(4*2)+(3*5)+(2*3)+(1*3)=150
150 % 10 = 0
So 79325-33-0 is a valid CAS Registry Number.

79325-33-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dichloro-2-(trichloromethyl)quinoline

1.2 Other means of identification

Product number -
Other names 3,4-dichloro-2-trichloromethylquinoline

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:79325-33-0 SDS

79325-33-0Upstream product

79325-33-0Downstream Products

79325-33-0Relevant academic research and scientific papers

Trichloromethylquinolines: Synthesis and Reaction with Trimethyl Phosphite

Kato, Tetsuzo,Katagiri, Nobuya,Wagai, Akihiro

, p. 1069 - 1075 (2007/10/02)

Heating of methylquinolines (1, 3, 6, and 12) with phosphorus pentachloride in phosphoryl chloride gave the corresponding trichloromethylquinoline derivatives (2, 4, 9, and 14).Similar treatment of 4-chloro-2-methyl-3-nitroquinoline (16) gave 4-chloro-2-dichloromethyl-3-nitroquinoline (17), 4-chloro-3-nitro-2-trichloromethylquinoline (18), and 3,4-dichloro-2-cyanoquinoline (19).The reaction of 2-trichloromethylquinolines (2, 9, and 18) with trimethyl phosphite gave the corresponding methylated products, 2-(1,1-dichloroethyl)quinolines (21, 24, and 27).However, 4-trichloromethylquinolines (4 and 14) reacted with trimethyl phosphite under similar conditions to give 4-dichloromethylquinolines (23 and 13).Keywords - chlorination; dichloromethylquinolines; trichloromethylquinolines; phosphorus pentachloride, phosphoryl chloride, trimethyl phosphite; methylation; phosphorylation; 2-(1,1-dichloroethyl)quinolines.

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