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2,3,5-Trichloro-6-(trichloromethyl)pyridine is a chemical compound belonging to the pyridine family, characterized by the molecular formula C7H2Cl6N. It is a highly toxic and environmentally persistent substance known for its potent and long-lasting effects on target organisms. Due to its hazardous nature, it requires careful handling and disposal with appropriate protective measures.

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  • 7041-24-9 Structure
  • Basic information

    1. Product Name: 2,3,5-Trichloro-6-(trichloromethyl)pyridine
    2. Synonyms: 2,3,5-Trichloro-6-(trichloromethyl)pyridine;Pyridine, 2,3,5-trichloro-6-(trichloromethyl)-
    3. CAS NO:7041-24-9
    4. Molecular Formula: C6HCl6N
    5. Molecular Weight: 299.7968
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 7041-24-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 308°Cat760mmHg
    3. Flash Point: 168.9°C
    4. Appearance: /
    5. Density: 1.765g/cm3
    6. Vapor Pressure: 0.00127mmHg at 25°C
    7. Refractive Index: 1.599
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,3,5-Trichloro-6-(trichloromethyl)pyridine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,3,5-Trichloro-6-(trichloromethyl)pyridine(7041-24-9)
    12. EPA Substance Registry System: 2,3,5-Trichloro-6-(trichloromethyl)pyridine(7041-24-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 7041-24-9(Hazardous Substances Data)

7041-24-9 Usage

Uses

Used in Pesticide Industry:
2,3,5-Trichloro-6-(trichloromethyl)pyridine is used as a pesticide for its potent and long-lasting effects on target organisms. It helps control pests and protect crops from damage, contributing to increased agricultural productivity.
Used in Herbicide Industry:
In the herbicide industry, 2,3,5-Trichloro-6-(trichloromethyl)pyridine is utilized for its ability to effectively control and eliminate unwanted plants and weeds. Its application ensures better crop growth and management by reducing competition for resources and preventing the spread of invasive species.

Check Digit Verification of cas no

The CAS Registry Mumber 7041-24-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,4 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7041-24:
(6*7)+(5*0)+(4*4)+(3*1)+(2*2)+(1*4)=69
69 % 10 = 9
So 7041-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C6HCl6N/c7-2-1-3(8)5(9)13-4(2)6(10,11)12/h1H

7041-24-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5-trichloro-6-(trichloromethyl)pyridine

1.2 Other means of identification

Product number -
Other names 2-(trichloromethyl)-3,5,6-trichloropyridine

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:7041-24-9 SDS

7041-24-9Downstream Products

7041-24-9Relevant articles and documents

HALOGEN-SUBSTITUTED PYRIDINES 4. 2,3,5-TRICHLOROPYRIDINES SUBSTITUTED AT POSITION 6

Shvekhgeimer, G. A.,Kobrakov, K. I.,Toshkhodzhaev, H. A.

, p. 572 - 575 (2007/10/02)

Addition of alkyl(aryl)trichloromethylketones to acrylonitrile in the presence of copper(I) chloride gave chlorine-substituted δ-oxonitriles.Cyclization of the latter was effected by the action of dry hydrogen chloride yielding the corresponding chlorine-

DESTRUCTIVE CHLORINATION OF 3,4,5-TRICHLORO-2-(TRICHLOROMETHYL)PYRIDINE

Emel'yanov, V. I.,Stul', B. Ya.,Korolev, B. M.

, p. 1168 - 1171 (2007/10/02)

The extensive destructive chlorination of 3,4,5-trichloro-2-(trichloromethyl)pyridine proceeds by both thermal (160-245 deg C) and photochemical pathways.Perchloropyridine, perchloropicoline, and carbon tetrachloride are formed.The chlorinated derivatives of pyridine are formed by the loss of the CCl3 group with its subsequent replacement by a chlorine atom.

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