337957-59-2

Usage

Uses

Used in Pharmaceutical Industry:
1-(4-methylphenyl)-1H-pyrazole-4-carbaldehyde is used as an intermediate in the synthesis of pharmaceuticals for its potential biological and pharmacological activities.
Used in Agrochemical Industry:
1-(4-methylphenyl)-1H-pyrazole-4-carbaldehyde is used in the development of agrochemicals, contributing to the creation of new compounds for agricultural applications.
Used in Organic Compounds Synthesis:
1-(4-methylphenyl)-1H-pyrazole-4-carbaldehyde is used as a building block in the preparation of various heterocyclic compounds, which are important in organic chemistry.
Used in Medicinal Chemistry and Drug Discovery:
1-(4-methylphenyl)-1H-pyrazole-4-carbaldehyde is utilized in medicinal chemistry and drug discovery for its potential to contribute to the development of new therapeutic agents.
Used in Research and Academic Laboratories:
1-(4-methylphenyl)-1H-pyrazole-4-carbaldehyde is used in research and academic settings for its versatile reactivity and synthetic utility, aiding in the advancement of scientific knowledge and the discovery of new chemical reactions.

InChI:InChI=1/C11H10N2O/c1-9-2-4-11(5-3-9)13-7-10(8-14)6-12-13/h2-8H,1H3

Upstream product

• 68-12-2 N,N-dimethyl-formamide 
• 100-97-0 hexamethylenetetramine 
• 539-44-6 N-4-methylphenylhydrazine 
• 20518-17-6 1-(4-methylphenyl)-1H-pyrazole 

Downstream Products

• 1373836-35-1 2-(1-(p-tolyl)pyrazol-4-yl)benzimidazole 
• 851180-85-3 (1-(4-methylphenyl)-1H-pyrazol-4-yl)methanol 
• 77458-34-5 p-methylphenyl-1H-pyrazole-4-ol 
• 1612877-07-2 (E)-2-(2-(1-(p-tolyl)-1H-pyrazol-4-yl)vinyl)quinolin-8-ol 
• 1612877-16-3 C₂₃H₁₉N₃O₂ 

Relevant academic research and scientific papers

SUBSTITUTED PYRAZOLE DERIVATIVES AS INSECTICIDES AND FUNGICIDES

An object of the present disclosure is to provide a novel substituted pyrazole compound or a salt thereof as represented by formula (1) that controls pests: wherein, Q represents an oxygen atom or a sulfur atom, or the like; R represents substituted or unsubstituted aryl, C1-C12alkyl, or the like; Represents hydrogen, substituted or unsubstituted C1- C12alkylcarbonyl, substituted or unsubstituted C1-C12alkoxycarbonyl or the like; R2and R3each independently represent hydrogen, substituted or unsubstituted C1-C12alkyl, or the like; R4and R5each independently represent hydrogen, substituted or unsubstituted C1- C12alkyl, or the like; andX1, X2and X3grepresent C-R8, C-Rg and C-R|0, respectively, wherein R8, R9and Rjgeach independently represent hydrogen, halogen, methyl, ethyl or the like. The compounds of formula (1) are useful as insecticides and fungicides.

Pyrazolyl pyrimidinyl ether compound and use thereof

The present invention discloses a pyrazolyl pyrimidinyl ether compound, the compound has a structure as shown in formula (I), and the substituent groups in the (I) are as defined in the specification. The pyrazolyl pyrimidinyl ether compound has broad-spectrum bactericidal activity, has good control effects on downy mildew of cucumber, anthracnose of cucumber, rice blast, cucumber gray mold and other diseases, and is especially better in the control effect on the anthracnose of cucumber,.

Chemoselective and regiospecific formylation of 1-phenyl-1H-pyrazoles through the duff reaction

The synthesis of formylated 1-phenyl-1H-pyrazole derivatives under the Duff reaction conditions is reported. Our results indicate that 1-phenyl-1H-pyrazole systems containing electron-withdrawing and electron-donating substituents at the phenyl moiety rea

Complete assignment of NMR data of 22 phenyl-1H-pyrazoles' derivatives

Complete assignment of 1H and 13C NMR chemical shifts and J(1H/1H and 1H/19F) coupling constants for 22 1-phenyl-1H-pyrazoles' derivates were performed using the concerted application of 1H 1D and 1H, 13C 2D gs-HSQC and gs-HMBC experiments. All 1-phenyl-1H-pyrazoles' derivatives were synthesized as described by Finar and co-workers. The formylated 1-phenyl-1H-pyrazoles' derivatives were performed under Duff's conditions. Copyright