Welcome to LookChem.com Sign In|Join Free
  • or
(4-methyl-2,6-dinitro-phenyl)-carbamic acid ethyl ester, commonly known as metolcarb, is a highly toxic chemical compound that functions as a pesticide and insecticide. It is effective in controlling various pests such as beetles, aphids, and caterpillars by disrupting their nervous systems, leading to their death.
Used in Agriculture:
Metolcarb is used as a pesticide and insecticide in the cultivation of fruits and vegetables to protect crops from damaging pests. Its high toxicity makes it a potent agent in controlling a variety of insects that can harm agricultural yields.
Used in Pest Control:
Metolcarb is utilized in pest control applications to manage and eliminate insect infestations. Its effectiveness in targeting the nervous systems of insects makes it a valuable tool in integrated pest management strategies.
Note: Due to the high toxicity of metolcarb, it is crucial to follow strict regulations and safety precautions during its use. Proper handling, storage, and disposal are essential to minimize the risk of exposure and potential harm to humans and the environment.

100663-78-3

Post Buying Request

100663-78-3 Suppliers

Recommended suppliers

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

100663-78-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100663-78-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,6,6 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 100663-78:
(8*1)+(7*0)+(6*0)+(5*6)+(4*6)+(3*3)+(2*7)+(1*8)=93
93 % 10 = 3
So 100663-78-3 is a valid CAS Registry Number.

100663-78-3Downstream Products

100663-78-3Relevant academic research and scientific papers

A Comparison of the Reactions of Some Ethyl N-Arylcarbamates with Those of the Corresponding Acetanilides. I. Nitration

Rosevear, Judi,Wilshire, John F. K.

, p. 723 - 733 (2007/10/02)

The reactions of some ethyl N-arylcarbamates and of the corresponding acetanilides towards 1 equiv. of sodium nitrate in concentrated sulfuric acid at 0-5 deg have been compared with one another and have been found to exhibit significant differences.Except in the case of the unsubstituted analogues, nitration of the carbamates was found to occur significantly more quickly than that of the acetanilides as shown by (i) a representative competitive nitration, and (ii) the fact the carbamates containing a nitro group are nitrated smoothly whereas the corresponding nitroacetanilides are slow to react.On the basis of competitive reactions, it is suggested that this difference in reactivity is due to steric factors.

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 100663-78-3