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2-(2,4-Dichlorophenoxy)ethanethioamide, commonly known as ethiofencarb, is an organothiophosphate compound and a member of the carbamate family. It is a chemical compound that functions as a pesticide and herbicide, inhibiting the enzyme acetylcholinesterase, which leads to the accumulation of acetylcholine in the nervous system of insects and pests, causing overstimulation, paralysis, and death.

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  • 2302-32-1 Structure
  • Basic information

    1. Product Name: 2-(2,4-DICHLOROPHENOXY)ETHANETHIOAMIDE
    2. Synonyms: 2-(2,4-Dichlorophenoxy)thioacetamide, 97%;2-(2,4-DICHLOROPHENOXY)ETHANETHIOAMIDE
    3. CAS NO:2302-32-1
    4. Molecular Formula: C8H7Cl2NOS
    5. Molecular Weight: 236.12
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2302-32-1.mol
  • Chemical Properties

    1. Melting Point: 139-141
    2. Boiling Point: 367.7 °C at 760 mmHg
    3. Flash Point: 176.2 °C
    4. Appearance: /
    5. Density: 1.452 g/cm3
    6. Vapor Pressure: 1.34E-05mmHg at 25°C
    7. Refractive Index: 1.634
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-(2,4-DICHLOROPHENOXY)ETHANETHIOAMIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(2,4-DICHLOROPHENOXY)ETHANETHIOAMIDE(2302-32-1)
    12. EPA Substance Registry System: 2-(2,4-DICHLOROPHENOXY)ETHANETHIOAMIDE(2302-32-1)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 2302-32-1(Hazardous Substances Data)

2302-32-1 Usage

Uses

Used in Pesticide Applications:
Ethiofencarb is used as an insecticide and miticide for controlling a variety of insect and mite pests on fruits, vegetables, and ornamental plants. Its mode of action involves the inhibition of acetylcholinesterase, disrupting the nervous system of pests and leading to their death.
Used in Herbicide Applications:
In the agricultural industry, ethiofencarb is utilized as a selective herbicide in rice cultivation. It is effective in controlling grassy weeds, thus ensuring the healthy growth of rice crops.
Used in Crop Protection:
Ethiofencarb plays a crucial role in crop protection by safeguarding plants from harmful insects and mites, thereby reducing crop damage and increasing agricultural productivity.

Check Digit Verification of cas no

The CAS Registry Mumber 2302-32-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,0 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2302-32:
(6*2)+(5*3)+(4*0)+(3*2)+(2*3)+(1*2)=41
41 % 10 = 1
So 2302-32-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H7Cl2NOS/c9-5-1-2-7(6(10)3-5)12-4-8(11)13/h1-3H,4H2,(H2,11,13)

2302-32-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H26583)  2-(2,4-Dichlorophenoxy)thioacetamide, 97%   

  • 2302-32-1

  • 250mg

  • 396.0CNY

  • Detail
  • Alfa Aesar

  • (H26583)  2-(2,4-Dichlorophenoxy)thioacetamide, 97%   

  • 2302-32-1

  • 1g

  • 1107.0CNY

  • Detail

2302-32-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,4-DICHLOROPHENOXY)ETHANETHIOAMIDE

1.2 Other means of identification

Product number -
Other names 2,6-DIHYDROXYTEREPHTHALIC ACID

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:2302-32-1 SDS

2302-32-1Relevant articles and documents

Synthesis and Antitubercular Activity of 4-(5-Nitro-2-furyl/2-pyrazinyl/1-adamantyl)-2-(alkyl/aryl/arylamino)thiazoles

Khadse, B. G.,Lokhande, S. R.,Bhamaria, R. P.,Prabhu, S. R.

, p. 856 - 860 (2007/10/02)

The reaction of haloketones, obtained from Arndt-Eistert reaction on the acid chlorides of 1-adamantane, 5-nitrofuroic acid and pyrazine-2-carboxylic acid, with different thioamides and thioureas affords the title thiazoles (I-III).Some of them exhibit interesting antitubercular activity at 6.25 to 0.38 μg/ml concentration against H37Rv strain of M. tubercolosis in vitro testing.The structure activity relationship (SAR) has also been discussed.

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