438450-38-5

Basic information

• Product Name: 3-chloro-2-(3-(trifluoromethyl)-1H-pyrazol-1-yl)pyridine
• Synonyms: 3-chloro-2-(3-(trifluoromethyl)-1H-pyrazol-1-yl)pyridine;3-chloro-2-(3-(trifluoromethyl)-1H-pyrazol-1-yl)pyridine（WS201749）
• CAS NO: 438450-38-5
• Molecular Formula: C₉H₅ClF₃N₃
• Molecular Weight: 248
• Mol File: 438450-38-5.mol
• Article Data: 17

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-chloro-2-(3-(trifluoromethyl)-1H-pyrazol-1-yl)pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-chloro-2-(3-(trifluoromethyl)-1H-pyrazol-1-yl)pyridine(438450-38-5)
• EPA Substance Registry System: 3-chloro-2-(3-(trifluoromethyl)-1H-pyrazol-1-yl)pyridine(438450-38-5)

Safety Data

• Hazardous Substances Data: 438450-38-5(Hazardous Substances Data)

Upstream product

• 22841-92-5 (3-chloro-2-pyridyl)hydrazine 
• 59938-06-6 4-ethoxy-1,1,1-trifluoro-3-butene-2-one 
• 1034303-16-6 (3-chloropyridin-2-yl)hydrazinehydrochloride 
• 354-32-5 trifluoracetyl chloride 
• 109-92-2 ethyl vinyl ether 
• 2402-77-9 2,3-dichloro-pyridine 
• 20154-03-4 3-(trifluoromethyl)pyrazole 

Downstream Products

• 438450-39-6 1-(3-chloro-2-pyridinyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxylic acid 
• 1422678-02-1 2-(3-chloro-2-pyridyl)-N-[2-methyl-4-chloro-6-[(cyclopropylmethylethyl-λ⁴-sulfanylidene)carbamoyl]phenyl]-5-(trifluoromethyl)pyrazole-3-carboxamide 
• 1422877-12-0 2-(3-chloro-2-pyridyl)-N-[2-methyl-4-cyano-6-[(dipentyl-λ4-sulfanylidene)carbamoyl]phenyl]-5-(trifluoromethyl)pyrazole-3-carboxamide 
• 1422677-87-9 2-(3-chloro-2-pyridyl)-N-[2-methyl-4-chloro-6-[(diethyl-λ⁴-sulfanylidene)carbamoyl]phenyl]-5-(trifluoromethyl)-2H-pyrazole-3-carboxamide 
• 1422677-86-8 2-(3-chloro-2-pyridyl)-N-[2,4-dichloro-6-[(bis-2-propyl-λ⁴-sulfanylidene)carbamoyl]phenyl]-5-(trifluoromethyl)-2H-pyrazole-3-carboxamide 
• 1422677-85-7 2-(3-chloro-2-pyridyl)-N-[2,4-dichloro-6-[(diethyl-λ⁴-sulfanylidene)carbamoyl]phenyl]-5-(trifluoromethyl)-2H-pyrazole-3-carboxamide 

Relevant articles and documents

Preparation methods for pyrazole compound

The invention discloses preparation methods for a pyrazole compound. The preparation methods include a method A and a method B. The method A comprises a step of subjecting a compound as shown in a formula (II-A) which is described in the specification and a compound as shown in a formula (III) which is described in the specification to a cyclization reaction in a solvent so as to obtain a compound as shown in a formula (I) which is described in the specification. The method B comprises a step of subjecting a compound as shown in a formula (II-B) which is described in the specification and the compound as shown in the formula (III) which is described in the specification to a cyclization reaction in a solvent so as to obtain the compound as shown in the formula (I) which is described in the specification. The preparation methods use cheap and easily available raw materials, are low in production cost, mild in reaction conditions, simple to operate, high in yield and purity of the target compound, green and environment-friendly, and more suitable for industrial production.

Method of controlling particular insect pests by applying anthranilamide compounds

This invention pertains to a method for controlling lepidopteran, homopteran, hemipteran, thysanopteran and coleopteran insect pests comprising contacting the insects or their environment with an arthropodicidally effective amount of a compound of Formula I, its N-oxide or an agriculturally suitable salt thereof wherein A and B and R1 through R8 are as defined in the disclosure. This invention further relates to a benzoxazinone compound of Formula 10 wherein R4 through R8 are as defined in the disclosure, useful for preparation of a compound of Formula I.

USE OF ANTHRANILAMIDE COMPOUNDS FOR REDUCING INSECT-VECTORED VIRAL INFECTIONS

The present invention relates to agricultural methods using anthranilamide compounds of formula (I) wherein R1, R2, R3, R4, R5, R6, R7 and k are as defined in the description; an