138479-47-7

Basic information

• Product Name: Benzaldehyde,2-(1H-pyrazol-1-yl)-
• Synonyms: 2-(Pyrazol-1-yl)benzaldehyde;2-Pyrazol-1-yl-benzaldehyde
• CAS NO: 138479-47-7
• Molecular Formula: C₁₀H₈N₂O
• Molecular Weight: 172.1833
• Mol File: 138479-47-7.mol
• Article Data: 8

Chemical Properties

• Melting Point: 58 °C
• Boiling Point: 316.5 °C at 760 mmHg
• Flash Point: 145.2 °C
• Appearance: Light yellow powder
• Density: 1.15 g/cm³
• Vapor Pressure: 0.000408mmHg at 25°C
• Refractive Index: 1.604
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: -0.26±0.10(Predicted)
• CAS DataBase Reference: Benzaldehyde,2-(1H-pyrazol-1-yl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde,2-(1H-pyrazol-1-yl)-(138479-47-7)
• EPA Substance Registry System: Benzaldehyde,2-(1H-pyrazol-1-yl)-(138479-47-7)

Safety Data

• Hazard Codes: Harmful:
• HazardClass: IRRITANT
• Hazardous Substances Data: 138479-47-7(Hazardous Substances Data)

Usage

General Description

Benzaldehyde, 2-(1H-pyrazol-1-yl)- is a chemical compound that consists of a benzene ring with an aldehyde group and a pyrazole ring attached to it. It is commonly used as a flavoring agent in the food industry, giving a strong almond-like aroma. It can also be used as a precursor in the synthesis of pharmaceuticals and agrochemicals. Additionally, it has been studied for its potential use as an antifungal and antimicrobial agent due to its inhibitory effects on certain microorganisms. Overall, Benzaldehyde, 2-(1H-pyrazol-1-yl)- has a wide range of applications in various industries and is of interest in research for its potential biological activities.

InChI:InChI=1/C10H8N2O/c13-8-9-4-1-2-5-10(9)12-7-3-6-11-12/h1-8H

Upstream product

• 288-13-1 NH-pyrazole 
• 446-52-6 2-Fluorobenzaldehyde 
• 6630-33-7 ortho-bromobenzaldehyde 
• 1126-00-7 1-phenylpyrazole 
• 741717-59-9 (2-(1H-pyrazol-1-yl)phenyl)methanol 

Downstream Products

• 1033804-95-3 4-chloro-6-[2,2,2-trifluoro-1-(2-pyrazol-1-yl-phenyl)ethoxy]pyrimidine 
• 1020045-42-4 α-phenyl-(2-(1H-pyrazol-1-yl))benzyl alcohol 
• 1033804-94-2 2,2,2-trifluoro-1-(2-pyrazol-1-yl-phenyl)ethanol 

Relevant articles and documents

Mildness in preparative conditions directly affects the otherwise straightforward syntheses outcome of Schiff-base isoniazid derivatives: Aroylhydrazones and their solvolysis-related dihydrazones

Aroylhydrazones are versatile compounds with a series of applications, from biological to technological spheres. The simplicity of their preparation allows for a great chemical variability and synthetic manageability. However, the process can be not as st

Aromatic C-H Methylation and Other Functionalizations via the Rh(III)-Catalyzed Migratory Insertion of Bis(phenylsulfonyl)carbene and Subsequent Transformations

The Rh(III)-catalyzed migratory insertion of bis(phenylsulfonyl)carbene into aromatic C-H bonds has been developed. A variety of bis(phenylsulfonyl)methyl derivatives were prepared with good yields under mild conditions. The methylated products were readily obtained after reductive desulfonylation. Furthermore, the diverse transformations of bis(phenylsulfonyl)methyl to trideuteriomethyl, aldehyde, and other functional groups were demonstrated.

CXCR4 INHIBITORS AND USES THEREOF

The present invention provides compounds, compositions thereof, and methods of using the same.