Welcome to LookChem.com Sign In|Join Free
  • or
2-(2,5-dichlorophenylamino)-4H-benzo[d][1,3]oxazin-4-one is a complex organic compound with the molecular formula C14H7Cl2NO3. It is characterized by a benzoxazinone core, which is a heterocyclic structure containing oxygen and nitrogen atoms, and a 2,5-dichlorophenylamino group attached to the 2-position. 2-(2,5-dichlorophenylamino)-4H-benzo[d][1,3]oxazin-4-one is known for its potential applications in the field of agrochemicals, particularly as a herbicide. It is designed to inhibit specific enzymes in plants, leading to their controlled growth or death. The chemical's structure and properties make it a candidate for targeted weed management, although its specific use and effectiveness would be subject to further research and development.

82594-82-9

Post Buying Request

82594-82-9 Suppliers

Recommended suppliers

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

82594-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82594-82-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,5,9 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 82594-82:
(7*8)+(6*2)+(5*5)+(4*9)+(3*4)+(2*8)+(1*2)=159
159 % 10 = 9
So 82594-82-9 is a valid CAS Registry Number.

82594-82-9Downstream Products

82594-82-9Relevant academic research and scientific papers

Efficient synthesis of 4H-benzo[d][1,3]oxazin-4-ones from anthranilic acids and aryl isoselenocyanates

Xie, Yuanyuan,Zhu, Dongmei

, p. 351 - 355 (2013/07/26)

A synthesis in good to excellent yields of 23 4H-benzo[d][1,3]oxazin-4- ones, 18 of which are novel, from monosubstituted anthranilic acids and variously substituted phenyl isoselenocyanates without using any harsh reagents has been developed. The Se powder precipitated during the reaction could be efficiently recycled for the preparation of the aryl isoselenocyanates.

Convenient Preparation of N-substituted 2-Amino-4H-3,1-benzoxazin-4-ones and 3-Substituted 2,4(1H,3H)-Quinazolinediones

Papadopoulos, E. P.,Torres, C. D.

, p. 269 - 272 (2007/10/02)

Room temperature of 2-(3-arylureido)benzoic acids (1) and methyl2-(3-alkyl-, or 3-arylureido)-benzoates (2) with concentrated sulfuric acid leads to N-substituted 2-amino-4H-3,1-benzoxazin-4-ones (3) in generally very good yields.The isomeric 3-substitute

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 82594-82-9