156261-32-4

Basic information

• Product Name: (2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL
• Synonyms: (2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL
• CAS NO: 156261-32-4
• Molecular Formula: C₁₄H₁₅NO
• Molecular Weight: 213.27
• Mol File: 156261-32-4.mol

Chemical Properties

• Melting Point: 107 °C(Solv: ethanol (64-17-5))
• Boiling Point: 396.1±37.0 °C(Predicted)
• Appearance: /
• Density: 1.148±0.06 g/cm3(Predicted)
• PKA: 13.67±0.20(Predicted)
• CAS DataBase Reference: (2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: (2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL(156261-32-4)
• EPA Substance Registry System: (2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL(156261-32-4)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 156261-32-4(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
(2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL is used as a building block for the synthesis of various bioactive molecules, contributing to the development of new compounds with potential applications across different industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL serves as a key intermediate in the development of pharmaceuticals. Its unique structure allows for the creation of novel drugs with potential therapeutic effects.
Used in Medicinal Chemistry:
(2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL is utilized in medicinal chemistry for the exploration of its potential interactions with biological targets, which may lead to the discovery of new drugs and treatments.
Used in Drug Development:
As a component in drug development, (2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL plays a crucial role in the formulation and optimization of new pharmaceutical agents, enhancing their efficacy and safety.
Safety Note:
It is important to handle (2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL with care and follow proper safety guidelines to minimize health and environmental risks associated with this chemical compound.

Upstream product

• 64-17-5 ethanol 
• 17852-28-7 2-amino-5-methylbenzophenone 
• 98-88-4 benzoyl chloride 

Downstream Products

• 6968-24-7 2,6-Dibromo-4-methylaniline 
• 100-52-7 benzaldehyde 
• 34848-53-8 N-(2-(hydroxy(phenyl)methyl)-4-methylphenyl)acrylamide 
• 1132806-00-8 3,6-dimethyl-4-phenylquinolin-2(1H)-one 

Relevant articles and documents

An efficient iron-promoted synthesis of 6H-indolo[2,3- b] quinolines and neocryptolepine derivatives

A facile and practical method for the preparation of 6H-indolo[2,3-b]quinolines and neocryptolepines was developed under the promotion of the easily available ferric trichloride, affording the desired products with moderate to good yields.