24310-46-1

Basic information

• Product Name: 1-[1-(4-methoxyphenyl)ethylidene]-2-phenylhydrazine
• CAS NO: 24310-46-1
• Molecular Formula: C₁₅H₁₆N₂O
• Molecular Weight: 240.3003
• Mol File: 24310-46-1.mol
• Article Data: 96

Chemical Properties

• Boiling Point: 367°C at 760 mmHg
• Flash Point: 175.8°C
• Density: 1.03g/cm³
• Vapor Pressure: 1.41E-05mmHg at 25°C
• Refractive Index: 1.55
• CAS DataBase Reference: 1-[1-(4-methoxyphenyl)ethylidene]-2-phenylhydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[1-(4-methoxyphenyl)ethylidene]-2-phenylhydrazine(24310-46-1)
• EPA Substance Registry System: 1-[1-(4-methoxyphenyl)ethylidene]-2-phenylhydrazine(24310-46-1)

Safety Data

• Hazardous Substances Data: 24310-46-1(Hazardous Substances Data)

Usage

Type of compound

Hydrazine derivative

Usage

Research and pharmaceutical applications

Investigation

Potential therapeutic properties, particularly in relation to the central nervous system

Structural similarity

Known psychoactive compounds

Status

Specific pharmacological effects and potential medical uses are still being studied

Safety

Proper handling and precautions should be taken when working with AB-MDPH

Upstream product

• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 100-63-0 phenylhydrazine 
• 768-60-5 4-methoxyphenylacetylen 
• 59-88-1 phenylhydrazine hydrochloride 

Downstream Products

• 5784-95-2 2-(4-methoxyphenyl)-1H-indole 
• 76112-13-5 5-Isonicotinyl-3-(p-methoxyphenyl)-1-phenylpyrazole 
• 1229555-47-8 5-(4-methoxyphenyl)-2-phenyl-2H-1,2,3-diazaphosphole 
• 372107-36-3 3-(4-methoxyphenyl)-1-phenyl-1H-pyrazole-4-carboxylic acid 
• 1393711-92-6 1,4-dihydro-4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)-2,6-dimethyl-pyridine-3,5-dicarbonitrile 
• 313050-26-9 1-phenyl-3-[3-(4-methoxyphenyl)-1-phenyl-4-pyrazolyl]prop-2-en-1-one 
• 380456-99-5 C₂₆H₂₂N₂O₃ 

Relevant articles and documents

N-Hydroxyphthalimidyl diazoacetate (NHPI-DA): A modular methylene linchpin for the C-H alkylation of indoles

Despite the extensive studies on the reactions between conventional diazocompounds and indoles, these are still limited by the independent synthesis of the carbene precursors, the specific catalysts, and the required multi-step manipulation of the products. In this work, we explore redox-Active carbenes in the expedited and divergent synthesis of functionalized indoles. NHPI-DA displays unusual efficiency and selectivity to yield insertion products that can be swiftly elaborated into boron and carbon substituents that are particularly problematic in carbene-mediated reactions.

Synthesis of lathyrane diterpenoid nitrogen-containing heterocyclic derivatives and evaluation of their anti-inflammatory activities

As our ongoing work on lathyrane diterpenoid derivatization, three series of lathyrane diterpenoid derivatives were designed and synthesized based combination principles, including pyrazole, thiazole and furoxan moieties. Biological evaluation indicated t

Design, synthesis and in vitro antitumor evaluation of novel pyrazole-benzimidazole derivatives

A series of novel pyrazole-benzimidazole derivatives (6–42) have been designed, synthesized and evaluated for their in vitro antiproliferative activity against the HCT116, MCF-7 and Huh-7 cell lines. Among them, compounds 17, 26 and 35 showed significant