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(3-METHYL-5-PHENYL-4-ISOXAZOLYL)METHANOL, with the molecular formula C11H11NO2, is a tertiary alcohol featuring an isoxazole ring—a five-membered heterocyclic ring that includes nitrogen and oxygen atoms. This chemical compound is recognized for its structural attributes, making it a valuable building block in the synthesis of pharmaceuticals and agrochemicals.

113826-87-2

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113826-87-2 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 (3-METHYL-5-PHENYL-4-ISOXAZOLYL)METHANOL.

Check Digit Verification of cas no

The CAS Registry Mumber 113826-87-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,8,2 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 113826-87:
(8*1)+(7*1)+(6*3)+(5*8)+(4*2)+(3*6)+(2*8)+(1*7)=122
122 % 10 = 2
So 113826-87-2 is a valid CAS Registry Number.
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

113826-87-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-methyl-5-phenyl-1,2-oxazol-4-yl)methanol

1.2 Other means of identification

Product number -
Other names (3-Methyl-5-phenyl-isoxazol-4-yl)-methanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:113826-87-2 SDS

113826-87-2Relevant academic research and scientific papers

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

Maestro, Alicia,Banez, Jose M.,Lopez, Juan A.,Romero-Avila, Maria Cristina

, p. 1104 - 1106 (2007/10/03)

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

Heck, Reinhard,Ofenloch, Roland,Wolf, Roland

, p. 62 - 64 (2007/10/02)

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

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