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ChemicalBook--->CAS DataBase List--->500008-45-7

500008-45-7

500008-45-7 Structure

500008-45-7 Structure
IdentificationBack Directory
[Name]

CHLOANTRANILIPROLE
[CAS]

500008-45-7
[Synonyms]

Coragen
Rynaxpyr
DPX E2Y45
Chlorantranilipol
CHLOANTRANILIPROLE
Clorantraniliprole
CHLORANTRANILIPROLE
Chlorantraniliprole 95%
Chlorantraniliprole [iso]
Chlorantraniliprole Standard
Chlorantraniliprole Solution, 1000ppm
Chlorantraniliprole 95% (Rynaxypyr, Coragen)
3-Bromo-4-chloro-1-(3-chloro-2-pyridyl)-2-methyl-6-(methylcarbamoyl)pyrazole-5-carboxanilide
3-Bromo-N-[4-chloro-2-methyl-6-[(methylamino)carbonyl]phenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide
[Molecular Formula]

C18H14BrCl2N5O2
[MDL Number]

MFCD11840831
[MOL File]

500008-45-7.mol
[Molecular Weight]

483.152
Chemical PropertiesBack Directory
[Melting point ]

approximate 225℃ (dec.)
[Boiling point ]

526.6±50.0 °C(Predicted)
[density ]

1.66±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

Chloroform: Slightly Soluble; DMSO: Slightly Soluble
[form ]

A solid
[pka]

10.19±0.70(Predicted)
[color ]

White to off-white
[LogP]

3.641 (est)
[CAS DataBase Reference]

500008-45-7
[EPA Substance Registry System]

1H-Pyrazole-5-carboxamide, 3-bromo-N-[4-chloro-2-methyl-6-[(methylamino)carbonyl]phenyl]-1-(3-chloro-2-pyridinyl)- (500008-45-7)
Hazard InformationBack Directory
[Uses]

Chlorantraniliprole is a pyrazolylpyridine insecticide and an activator of insect ryanodine receptor.
[Definition]

ChEBI: A carboxamide resulting from the formal condensation of the carboxylic acid group of 3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylic acid with the primary amino group of 2-amino-5-chloro-N,3-dimethylbenzamide The first of the anthranilic diamide insecticides, it is a ryanodine receptor activator and is used to protect a wide variety of crops, including corn, cotton, grapes, rice and potatoes.
[Chemical Properties]

White crystal, specific gravity (for liquid) 1.507g/mL, melting point 208-210℃, decomposition temperature 330℃, vapor pressure (under 20~25) 6.3×1012Pa, solubility (under 20~25, mg/L): water 1.023, acetone 3.446, methanol 1.714, acetonitrile 0.711, ethyl acetate 1.144. Chlorfenvinphos It is highly efficient and broad-spectrum, and has good control effect on Lepidoptera of Noctuidae, stem borer moths, fruit moths, leaf roller moths, pink moths, vegetable moths, wheat moths, and fine moths, etc. It can also control Sphingidae weevils, leaf beetles; Diptera subterranean flies; sooty fly and many other non-lepidopteran pests.
[Preparation]

Chlorantraniliprole was synthesized by reaction of 3-bromo-1-(3-chloropyridin-2-pyridinyl)-1H-pyrazole-5carboxylic acid with 2-amino-5-chloro-3-methylbenzoic acid.3-bromo-1-(3-chloropyridin-2-pyridinyl)-1H-pyrazole5-carboxylic acid was prepared by reaction of maleic anhydride with 2,3-dichloropyridine as starting materials in eight steps.2-Amino-5-chloro-3-methylbenzoic acid was prepared by reaction of 2-amino-3-methylbenzoic acid in one step.The structure of target compound was conf irmed by 1H NMR.Total yield was 36.3%(calculated with 2,3-dichloropyridine),and purity determined by HPLC was over 95%.
[storage]

Store at -20°C
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-36/37
[Safety Statements ]

26
[Hazardous Substances Data]

500008-45-7(Hazardous Substances Data)
Spectrum DetailBack Directory
[Spectrum Detail]

Chlorantraniliprole(500008-45-7)1HNMR
Questions And AnswerBack Directory
[Description]

Chlorantraniliprole (Rynaxpyr) is an insecticide of the ryanoid class. It is a new compound by DuPont belonging to a new class of selective insecticides (anthranilic diamides) featuring a novel mode of action (group 28 in the IRAC classification). It is the first anthranilic diamide registered for use on turfgrass and landscape ornamentals. It is used to control a broad spectrum of pests including cabbage loopers, corn borers, Colorado potato beetle, European grapevine moth, armyworms and cutwormson a range of crops including potatoes and cotton. Its mechanism of action is through activating the insect ryanodine receptors (RyRs), further stimulating the release and depletion of intracellular calcium stores from the sarcoplasmic reticulum of muscle cells, causing impaired muscle regulation, paralysis and ultimately death of sensitive species.
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