736995-63-4

Basic information

• Product Name: 2-[1-(3-chloropyridine-2-yl)-3-bromo-1H-pyrazole-5-yl]-6-iodo-8-methyl-4H-3,1-benzoxazine-4-one
• Synonyms: 2-[1-(3-chloropyridine-2-yl)-3-bromo-1H-pyrazole-5-yl]-6-iodo-8-methyl-4H-3,1-benzoxazine-4-one
• CAS NO: 736995-63-4
• Molecular Weight: 543.546
• Mol File: 736995-63-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-[1-(3-chloropyridine-2-yl)-3-bromo-1H-pyrazole-5-yl]-6-iodo-8-methyl-4H-3,1-benzoxazine-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[1-(3-chloropyridine-2-yl)-3-bromo-1H-pyrazole-5-yl]-6-iodo-8-methyl-4H-3,1-benzoxazine-4-one(736995-63-4)
• EPA Substance Registry System: 2-[1-(3-chloropyridine-2-yl)-3-bromo-1H-pyrazole-5-yl]-6-iodo-8-methyl-4H-3,1-benzoxazine-4-one(736995-63-4)

Safety Data

• Hazardous Substances Data: 736995-63-4(Hazardous Substances Data)

Usage

Molecular structure

Consists of a pyridine and pyrazole moiety, as well as an oxazine ring.

Halogen substitutions

Contains chlorine, bromine, and iodine atoms.

Reactivity

High reactivity due to the presence of multiple halogens.

Potential for chemical reactions

The presence of multiple heterocyclic rings and halogens allows for diverse chemical reactions.

Applications

May have applications in pharmaceuticals, materials science, and organic synthesis.

Bioactive properties

The structure suggests that it may have bioactive properties.

Further research

More research is needed to fully understand the potential uses and properties of this chemical.

Upstream product

• 500011-86-9 3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxylic acid 
• 108857-24-5 2-amino-5-iodo-3-methylbenzoic acid 
• 4389-45-1 3-methylantranilic acid 

Relevant articles and documents

POLYSUBSTITUTED PYRIDYL PYRAZOLECARBOXAMIDE AND PREPARATION METHOD AND USE THEREOF

The present invention discloses a polysubstituted pyridyl pyrazolecarboxamide and its preparation method and use. The structure of the polysubstituted pyridyl pyrazolecarboxamide of the present invention is shown in the following General Formula I. The po

Rynaxypyr: A new insecticidal anthranilic diamide that acts as a potent and selective ryanodine receptor activator

Rynaxypyr is a highly potent and selective activator of insect ryanodine receptors with exceptional activity on a broad range of Lepidoptera. A strong correlation between insecticidal activity and ryanodine receptor activation is observed along with selective activity against insect over mammalian receptors. The synthesis and biological results are presented.

CYANO ANTHRANILAMIDE INSECTICIDES

This invention provides compounds of Formula (I), N -oxides and suitable salts thereof INSERT FORMULA I HERE wherein R1 is Me, Cl, Br or F; R2 is F, Cl, Br, C1-C4 haloalkyl or C1-C4 haloalkoxy; R3 is F, Cl or Br; R4 is H or C1-C4 alkyl,C3-C4 alkenyl, C3-C4 alkynyl, C3-C5 cycloalkyl, or C4-C6 cycloalkylalkyl, each optionally substituted with one substituent selected from the group consisting of halogen, CN, SMe S(O)Me, S(O)2Me and OMe; R5 is H or Me; R6 is H, F or Cl; and R7 is H, F or Cl. Also disclosed are methods for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound of Formula (I), anN-oxide thereof or a suitable salt of the compound (e.g., as a composition described herein). This invention also pertains to a composition for controlling an invertebrate pest comprising a biologically effective amount of a compound of Formula (I), an N-oxide thereof or a suitable salt of the compound and at least one additional component selected from the group consisting of a surfactant, a solid diluent and a liquid diluent.