871239-15-5

Basic information

• Product Name: 1H-Pyrazole-5-carboxylic acid, 3-broMo-1-(2-chlorophenyl)-4,5-dihydro-, Methyl ester
• Synonyms: 1H-Pyrazole-5-carboxylic acid, 3-broMo-1-(2-chlorophenyl)-4,5-dihydro-, Methyl ester;Methyl 3-bromo-1-(2-chlorophenyl)-4,5-dihydro-1H-pyrazole-5-carboxylate
• CAS NO: 871239-15-5
• Molecular Formula: C₁₁H₁₀BrClN₂O₂
• Molecular Weight: 317.5663
• Mol File: 871239-15-5.mol

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1H-Pyrazole-5-carboxylic acid, 3-broMo-1-(2-chlorophenyl)-4,5-dihydro-, Methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrazole-5-carboxylic acid, 3-broMo-1-(2-chlorophenyl)-4,5-dihydro-, Methyl ester(871239-15-5)
• EPA Substance Registry System: 1H-Pyrazole-5-carboxylic acid, 3-broMo-1-(2-chlorophenyl)-4,5-dihydro-, Methyl ester(871239-15-5)

Safety Data

• Hazardous Substances Data: 871239-15-5(Hazardous Substances Data)

Usage

Molecular weight

314.57 g/mol

Class

Pyrazole derivative

Substitution

Bromo and chloro-substituted phenyl ring

Biological activities

Potential medicinal properties

Common uses

Pharmaceutical and research applications

Upstream product

• 871239-14-4 (2-chlorophenyl)carbonohydrazonic dibromide 
• 292638-85-8 acrylic acid methyl ester 
• 871239-13-3 (2E)-[(2-chlorophenyl)hydrazono]acetic acid 
• 41052-75-9 o-chlorophenylhydrazine hydrochloride 

Downstream Products

• 871239-16-6 methyl 3-bromo-1-(2-chlorophenyl)-1H-pyrazole-5-carboxylate 
• 886583-56-8 3-bromo-N-[4-chloro-2-[[(1-cyclopropylethyl)amino]carbonyl]-6-methylphenyl]-1-(2-chlorophenyl)-1H-pyrazole-5-carboxamide 
• 871239-17-7 3-bromo-1-(2-chlorophenyl)-1H-pyrazole-5-carboxylic acid 
• 886583-61-5 2-[3-bromo-1-(2-chlorophenyl)-1H-pyrazol-5-yl]-6-chloro-8-methyl-4H-3,1-benzoxazin-4-one 

Relevant articles and documents

Anthranilamide insecticides

Disclosed are intermediate compounds for use in the synthesis of compounds of Formula 1, including all geometric and stereoisomers, N-oxides, and salts thereof, wherein J is a phenyl optionally substituted with one to four substituents independently selected from R5; or J is a heterocyclic ring selected from the group consisting of J-1 to J-8; R4 is C4-C12 alkylcycloalkyl, C5-C12 alkenylcycloalkyl, C5-C12 alkynylcycloalkyl, C4-C12 cycloalkylalkyl, C5-C12 cycloalkylalkenyl, C5-C12 cycloalkylalkynyl, C4-C12 cycloalkenylalkyl or C4-C12 alkylcycloalkenyl; each optionally substituted with one to six substituents selected from CH3 and halogen; or R4 is C3-C5 oxiranylalkyl, C3-C5 thiiranylalkyl, C4-C6 oxetanylalkyl, C4-C6 thietanylalkyl, 3-oxetanyl or 3-thietanyl, each optionally substituted with one to five substituents independently selected from C1-C3 alkyl, C1-C3 haloalkyl, halogen, CN, C2-C4 alkoxycarbonyl and C2-C4 haloalkoxycarbonyl; or R4 is C3-C5 aziridinylalkyl, C4-C6 azetidinylalkyl or 3-azetidinyl, each with R10 attached to the nitrogen atom, and optionally substituted on carbon atoms with one to five substituents independently selected from C1-C3 alkyl, C1-C3 haloalkyl, halogen, CN, C2-C4 alkoxycarbonyl and C2-C4 haloalkoxycarbonyl; and R1a R1b R2 R3 and R5 are as defined in the disclosure.

ANTHRANILAMIDE INSECTICIDES

This invention provides compounds of Formula 1, N oxides and suitable salts thereof, wherein R1 is Me, Cl, Br or I; R 2 is Cl, Br, I or -CN; R3 is Cl, Br, CF3, OCH2CF3 or OCF2H;