890707-29-6

Basic information

• Product Name: 2-AMino-5-cyano-N,3-diMethylbenzaMide
• Synonyms: 2-AMino-5-cyano-N,3-diMethylbenzaMide
• CAS NO: 890707-29-6
• Molecular Formula: C10H11N3O
• Molecular Weight: 189.21384
• Mol File: 890707-29-6.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 359.2±42.0 °C(Predicted)
• Appearance: /
• Density: 1.20±0.1 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• Solubility: DMSO (Slightly), Methanol (Slightly)
• PKA: 14.57±0.46(Predicted)
• CAS DataBase Reference: 2-AMino-5-cyano-N,3-diMethylbenzaMide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMino-5-cyano-N,3-diMethylbenzaMide(890707-29-6)
• EPA Substance Registry System: 2-AMino-5-cyano-N,3-diMethylbenzaMide(890707-29-6)

Safety Data

• Hazardous Substances Data: 890707-29-6(Hazardous Substances Data)

Usage

Description

2-Amino-5-cyano-N,3-dimethylbenzamide is a chemical compound that belongs to the cyano anthranilamide family. It is an impurity of Cyantraniliprole (C987580), a widely used insecticide with activity against invertebrate pests. 2-AMino-5-cyano-N,3-diMethylbenzaMide activates cyanodine receptors, leading to mortality in target pests.

Uses

Used in Pest Control Industry:
2-Amino-5-cyano-N,3-dimethylbenzamide is used as an impurity in the production of Cyantraniliprole, a potent insecticide. It contributes to the overall effectiveness of the insect control chemical by activating cyanodine receptors in invertebrate pests, causing their mortality. This makes it a valuable component in the development and formulation of insecticides targeting a broad range of pests.

Upstream product

• 890707-30-9 2-amino-5-bromo-N,3-dimethylbenzamide 
• 557-21-1 dicyanozinc 
• 143-33-9 sodium cyanide 
• 890707-28-5 2-amino-3-methyl-5-chlorobenzoyl-N-methylamine 
• 151-50-8 potassium cyanide 
• 773837-37-9 sodium cyanide 
• 1417858-21-9 pentyl 2-amino-5-bromo-3-methylbenzoate 
• 1032667-90-5 ethyl 2-amino-5-cyano-3-methylbenzoate 
• 74-89-5 methylamine 
• 1417858-33-3 benzyl 2-amino-5-cyano-3-methylbenzoate 
• 1417858-27-5 pentyl 2-amino-5-cyano-3-methylbenzoate 
• 1417858-28-6 hexyl 2-amino-5-cyano-3-methylbenzoate 
• 1417858-29-7 2-ethylhexyl 2-amino-5-cyano-3-methylbenzoate 
• 1417858-30-0 ethane-1,2-diyl 2-amino-5-cyano-3-methylbenzoate 

Relevant articles and documents

A PROCESS FOR THE SYNTHESIS OF ANTHRANILIC ACID/AMIDE COMPOUNDS AND INTERMEDIATES THEREOF

The present invention disclosed a process for the synthesis of compound of formula (Z) or a salt thereof, wherein, R, R1, R2, R3 and R10 are as defined in the detailed description. The process further comprises the synthesis of an anthranilic diamide compound of formula (I).

Cyan dihalogenation pyrazol amide series compound and preparation method and application thereof

The invention discloses a cyan dihalogenation pyrazol amide series compound and a preparation method and application thereof. The general chemical molecular formula of the compound is CHNOClBrR1R2, wherein R1 represents methyl, Cl or Br; R

PROCESS FOR PREPARING 2-AMINO-5-CYANOBENZOIC ACID DERIVATIVES

Disclosed is a method for preparing a compound of Formula 1 comprising (1) contacting a compound of Formula 2, with (2) at least one alkali metal cyanide and (3) at least one compound of Formula (4); wherein R1 is NHR3 or OR4; R2 is CH3 or Cl; R3 is H, C1-C4 alkyl, cyclopropyl, cyclopropylcyclopropyl, cyclopropylmethyl or methylcyclopropyl; R4 is H or C1-C4 alkyl; and X is Br, Cl or I. Also disclosed is a method for preparing a compound of Formula (4 )comprising contacting a mixture of (i) at least one compound of Formula (9 )and (ii) at least one metal reducing agent with (iii) dichlorobis(triphenylphosphine)nickel, and further disclosed is a method for removing nickel impurities from a mixture thereof with compounds of Formula (1 )comprising contacting the mixture with oxygen in the presence of an aqueous cyanide solution, and additionally disclosed is a method for preparing a compound of Formula (5); wherein R5, R6, R7 and Z are as defined in the disclosure, using a compound of Formula (1,) characterized by preparing the compound of Formula (1) by the method disclosed above.