Welcome to LookChem.com Sign In|Join Free
  • or
AcetaMide, 2,2,2-trichloro-N-(3-chlorophenyl)-, also known as 2,2,2-trichloro-N-(3-chlorophenyl)acetamide, is a chemical compound with the molecular formula C8H6Cl4NO. It is a derivative of acetamide, featuring a chlorophenyl group attached to the nitrogen atom and three chlorine atoms on the acetamide backbone. AcetaMide, 2,2,2-trichloro-N-(3-chlorophenyl)- is primarily used as an intermediate in the synthesis of various agrochemicals and pharmaceuticals, particularly in the production of herbicides and insecticides. Due to its chemical structure, it exhibits properties such as high reactivity and potential toxicity, necessitating proper handling and disposal protocols.

3004-73-7

Post Buying Request

3004-73-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

3004-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3004-73-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,0 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3004-73:
(6*3)+(5*0)+(4*0)+(3*4)+(2*7)+(1*3)=47
47 % 10 = 7
So 3004-73-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H5Cl4NO/c9-5-2-1-3-6(4-5)13-7(14)8(10,11)12/h1-4H,(H,13,14)

3004-73-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-Trichloro-N-(3-chlorophenyl)acetamide

1.2 Other means of identification

Product number -
Other names 3-Chlor-N-trichloracetyl-anilin

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:3004-73-7 SDS

3004-73-7Relevant academic research and scientific papers

Synthesis and antibacterial activities of pleuromutilin derivatives containing aryl urea groups

Zhang, Yuanyuan,Yang, Weiqing,Xu, Keping,Ma, Menglin,Wang, Yuliang

, p. 219 - 225 (2013/05/22)

A series of novel pleuromutilin derivatives containing aryl urea groups was synthesized and their antibacterial activities were evaluated in vitro against S. aureus ATCC 26113, S.aureus SC, S. albus ATCC 8799 and P. aeruginosa ATCC 27853. Most of compound

Formation of N-Substituted Trichloroacetamides from Amines and Hexachloroacetone

Bew, Clive,Joshi, Virginia Otero de,Gray, Jim,Kaye, Perry T.,Meakins, G. Denis

, p. 945 - 948 (2007/10/02)

Procedures are described for converting primary amines into their well-crystalline trichloroacetyl-derivatives by treatment with hexachloroacetone under mild conditions.Although secondary aromatic N-methylamines are unaffected by hexachloroacetone, saturated heterocyclic amines react vigorously.A mechanistic study using 2-amino-4-t-butylthiazole showed that the reaction is first order in hexachloroacetone, second order in amine, and base-catalysed; there is no appreciable kinetic isotope (H/D) effect nor accumulation of intermediates during the reaction.A sequence which accommodates these results is suggested.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 3004-73-7