113826-87-2

Basic information

• Product Name: (3-METHYL-5-PHENYL-4-ISOXAZOLYL)METHANOL
• Synonyms: BUTTPARK 95\50-100;(3-METHYL-5-PHENYL-4-ISOXAZOLYL)METHANOL;(3-METHYL-5-PHENYLISOXAZOL-4-YL)METHANOL;RARECHEM AL BD 1293;(3-Methyl-5-phenyl-1,2-oxazol-4-yl)methanol, 4-(Hydroxymethyl)-3-methyl-5-phenylisoxazole
• CAS NO: 113826-87-2
• Molecular Formula: C₁₁H₁₁NO₂
• Molecular Weight: 189.21
• Mol File: 113826-87-2.mol

Chemical Properties

• Melting Point: 109 °C
• Boiling Point: 379.4°Cat760mmHg
• Flash Point: 183.2°C
• Appearance: /
• Density: 1.176g/cm³
• Vapor Pressure: 1.97E-06mmHg at 25°C
• Refractive Index: 1.566
• CAS DataBase Reference: (3-METHYL-5-PHENYL-4-ISOXAZOLYL)METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: (3-METHYL-5-PHENYL-4-ISOXAZOLYL)METHANOL(113826-87-2)
• EPA Substance Registry System: (3-METHYL-5-PHENYL-4-ISOXAZOLYL)METHANOL(113826-87-2)

Safety Data

• Safety Statements: 22-24/25
• HazardClass: IRRITANT
• Hazardous Substances Data: 113826-87-2(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
(3-METHYL-5-PHENYL-4-ISOXAZOLYL)METHANOL is utilized as a key intermediate in the synthesis of various pharmaceuticals due to its unique structural features that can be incorporated into drug molecules to enhance their therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, (3-METHYL-5-PHENYL-4-ISOXAZOLYL)METHANOL serves as a fundamental component in the creation of compounds designed to protect crops and control pests, leveraging its reactive functional groups for the development of effective agrochemicals.
Used in Materials Science:
(3-METHYL-5-PHENYL-4-ISOXAZOLYL)METHANOL may find applications in materials science, where its structural characteristics could contribute to the development of new materials with specific properties, such as improved stability or reactivity.
Used in Organic Chemistry:
As a versatile organic compound, (3-METHYL-5-PHENYL-4-ISOXAZOLYL)METHANOL is employed in organic chemistry for various reactions and synthesis processes, taking advantage of its reactivity and the presence of the isoxazole ring to form complex organic molecules.
It is crucial to handle (3-METHYL-5-PHENYL-4-ISOXAZOLYL)METHANOL with caution, considering its potential health and environmental risks if mismanaged or improperly disposed of. Proper safety measures and disposal protocols should be strictly adhered to in all applications of this compound.

InChI:InChI=1/C11H11NO2/c1-8-10(7-13)11(14-12-8)9-5-3-2-4-6-9/h2-6,13H,7H2,1H3

Upstream product

• 17153-21-8 3-methyl-5-phenyl-isoxazole-4-carboxylic acid 

Downstream Products

• 50698-90-3 N-(3-methyl-5-phenyl-isoxazol-4-ylmethyl)-phthalimide 
• 89479-66-3 3-Methyl-5-phenyl-isoxazole-4-carbaldehyde 
• 213024-96-5 4-(Chloromethyl)-3-methyl-5-phenylisoxazole 

Relevant articles and documents

Synthesis of (isoxazol-4-ylmethyl)triphenylphosphonium salts derived from 5-alkyiand 5-aryl-3-methylisoxazoles

The synthesis of (isoxazol-4-ylmethyl)triphenylphosphonium salts derived from 5-alkyl- and 5-aryl-3-methylisoxazoles has been carried out. This method involves the preparation of several 4-(chloromethyl)isoxazoles which are suitable precusors for these phosphonium salts. The phosphonium salts were completely characterized by spectroscopic methods and were obtained in very good to quantitative yields.

Eine verbesserte Methode zur Synthese substituierter Isoxazol-4-carbaldehyde

A series of isoxazole-4-carbaldehydes 3 have been readily prepared by simple oxidation of the corresponding isoxazolylalcohols 2 with sodium dichromate in dimethylsulfoxide.