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2-ISOXAZOL-3-YL-PHENOL, also known as 2-isoxazol-3-ylphenol, is a chemical compound with the molecular formula C10H7NO2. It is a phenolic compound that contains both an isoxazole ring and a phenol group. This chemical is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It can also be used as a precursor for the development of potential drugs for various diseases. 2-ISOXAZOL-3-YL-PHENOL has also shown antimicrobial and antioxidant properties, making it a potential candidate for the development of new drugs and agrochemicals.

61348-48-9

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61348-48-9 Usage

Uses

Used in Pharmaceutical Industry:
2-ISOXAZOL-3-YL-PHENOL is used as a building block for the synthesis of various pharmaceuticals due to its unique structure and reactivity.
Used in Agrochemical Industry:
2-ISOXAZOL-3-YL-PHENOL is used as a building block for the synthesis of various agrochemicals due to its unique structure and reactivity.
Used in Drug Development:
2-ISOXAZOL-3-YL-PHENOL is used as a precursor for the development of potential drugs for various diseases.
Used in Antimicrobial Applications:
2-ISOXAZOL-3-YL-PHENOL is used as an antimicrobial agent due to its antimicrobial properties.
Used in Antioxidant Applications:
2-ISOXAZOL-3-YL-PHENOL is used as an antioxidant agent due to its antioxidant properties.

Check Digit Verification of cas no

The CAS Registry Mumber 61348-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,4 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61348-48:
(7*6)+(6*1)+(5*3)+(4*4)+(3*8)+(2*4)+(1*8)=119
119 % 10 = 9
So 61348-48-9 is a valid CAS Registry Number.

61348-48-9SDS

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 6-(1,2-oxazol-3-ylidene)cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names 3-o-Hydroxyphenylisoxazol

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:61348-48-9 SDS

61348-48-9Relevant academic research and scientific papers

THE REACTIONS OF CHROMONE AND 2-HYDROXYCHROMANONE WITH HYDROXYLAMINE

Szabo, Vince,Borbely, Janos,Theisz, Edit,Borda, Jeno,Janzso, Geza

, p. 413 - 417 (2007/10/02)

Chromone and 2-hydroxychromanone react with hydroxylamine to give several products through attack at Ca2.The aldoxime 2 is transformed to dioxime 4 or to isoxazole 3.The dioxime exists as a tautomer mixture; it reacts in several ways, giving chromoneoxime

A NEW PATHWAY IN THE REACTIONS OF CHROMONES AND HYDROXYLAMINE IN ANHYDROUS SOLUTIONS

Szabo, Vince,Borbely, Janos,Theisz, Edit,Janzso, Geza

, p. 5347 - 5350 (2007/10/02)

In the nucleophilic reaction of chromone (1) with NH2OH.HCl in anhydrous methanol a new compound 2-methoxychromanone (6) appeared as an intermediate in the formation of chromone oxime (8) and 2-methoxychromanone oxime (7).

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