2644-94-2

Basic information

• Product Name: 1-BENZYL-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE
• Synonyms: 1H-Pyrazole-4-carboxaldehyde,3,5-diMethyl-1-(phenylMethyl)-
• CAS NO: 2644-94-2
• Molecular Formula: C₁₃H₁₄N₂O
• Molecular Weight: 214.27
• Mol File: 2644-94-2.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 376.7 °C at 760 mmHg
• Flash Point: 181.6 °C
• Appearance: /
• Density: 1.09 g/cm³
• Vapor Pressure: 7.13E-06mmHg at 25°C
• Refractive Index: 1.576
• CAS DataBase Reference: 1-BENZYL-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BENZYL-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE(2644-94-2)
• EPA Substance Registry System: 1-BENZYL-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE(2644-94-2)

Safety Data

• Hazardous Substances Data: 2644-94-2(Hazardous Substances Data)

Usage

General Description

1-Benzyl-3,5-dimethyl-1H-pyrazole-4-carbaldehyde is a chemical compound with a complex molecular structure that belongs to the class of pyrazole derivatives. It is a yellow solid substance that is commonly used as an intermediate in the synthesis of pharmaceuticals and organic compounds. 1-BENZYL-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE has potential applications in the field of medicinal chemistry due to its ability to interact with biological molecules and exhibit pharmacological activities. Its unique structure makes it an important building block for the development of new drugs and biologically active compounds. Additionally, it has been studied for its potential use in the synthesis of materials with specific properties and functions in various industrial applications.

InChI:InChI=1/C13H14N2O/c1-10-13(9-16)11(2)15(14-10)8-12-6-4-3-5-7-12/h3-7,9H,8H2,1-2H3

Upstream product

• 20570-96-1 benzylhydrazine dihydrochloride 
• 123-54-6 acetylacetone 
• 1134-81-2 1-benzyl-3,5-dimethyl-1H-pyrazole 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 1303527-00-5 2,2'-{[(1-benzyl-3,5-dimethyl-1H-pyrazol-4-yl)methanediyl]di(sulfanediyl)}diethanol hydrochloride 
• 6569-34-2 1,2-diselenacyclopentane 
• 1367597-40-7 1-benzyl-3,5-dimethyl-4-(1,3-oxathiolan-2-yl)-1H-pyrazole hydrochloride 
• 1303644-24-7 2,2'-{[(1-benzyl-3,5-dimethyl-1H-pyrazol-4-yl)methanediyl]di(sulfanediyl)}diethanol 
• 1369592-25-5 4-(1,3-diselenan-2-yl)-3,5-dimethyl-1-prop-2-en-1H-pyrazole 
• 1356914-70-9 C₁₇H₂₂N₂OS₂ 
• 1356914-75-4 C₁₅H₁₈N₂OS 
• 2764-61-6 4-(1-benzyl-3,5-dimethyl-1H-pyrazol-4-ylmethylene)-2-phenyl-4H-oxazol-5-one 

Relevant articles and documents

2-(pyrazol-4-yl)-1,3-oxaselenolanes from pyrazole carbaldehydes and 2-selanyl-1-ethanol

Pyrazole carbaldehydes react with 2-selanyl-1-ethanol at room temperature in the presence of trimethylchlorosilane followed by treatment C with triethyl amine to afford the corresponding 2-(pyrazol-4-yl)-1,3-oxaselenolanes. The structure of the novel compounds was confirmed by IR, 13 C, 1 H, 15N, and 77 Se NMR spectroscopy.this article online at wileyonlinelibrary.com.

Fragmentation of pyrazolecarbaldehyde thio- and dithioacetals under electron impact and chemical ionization

The mass spectra of 1-substituted 3,5-dimethyl-1H-pyrazole-4-carbaldehyde bis(2-hydroxyethyl) dithioacetals and thioacetals were studied for the first time. The main fragmentation pathways of their molecular ions generated under electron impact and chemic

2-[4-(PYRAZOL-4-YLALKYL)PIPERAZIN-1-YL]-3-PHENYL PYRAZINES AND PYRIDINES AND 3-[4-(PYRAZOL-4-YLALKYL)PIPERAZIN-1-YL]-2-PHENYL PYRIDINES AS 5-HT7 RECEPTOR ANTAGONISTS

The present invention provides selective 5-HT7 receptor antagonist compounds of Formula I and their use in the treatment of migraine, persistent pain, and anxiety: where A and B are each independently C(H)= or N=, provided that at least one of A and B is -N=, n is 1-3, m is 0-3, and R14 are as defined herein.