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4-BROMO-2-(5-ISOXAZOLYL)PHENOL is a chemical compound characterized by the molecular formula C9H6BrNO2. It is a brominated derivative of 5-isoxazolylphenol, known for its antimicrobial properties and potential applications in various fields, including pharmaceuticals and agrochemicals. 4-BROMO-2-(5-ISOXAZOLYL)PHENOL also serves as a building block in the synthesis of organic compounds and functions as a reagent in chemical reactions. Due to its hazardous nature, it requires careful handling and storage.

213690-27-8

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213690-27-8 Usage

Uses

Used in Pharmaceutical Industry:
4-BROMO-2-(5-ISOXAZOLYL)PHENOL is used as an intermediate in the synthesis of pharmaceuticals for its potential anti-inflammatory and antiviral properties. Its unique structure allows for the development of new drugs that can target specific biological pathways and address various health conditions.
Used in Agrochemical Industry:
In the agrochemical industry, 4-BROMO-2-(5-ISOXAZOLYL)PHENOL is utilized as a building block in the synthesis of agrochemicals, such as pesticides and herbicides. Its antimicrobial properties contribute to the development of effective solutions for crop protection and management of pests and diseases.
Used in Organic Synthesis:
4-BROMO-2-(5-ISOXAZOLYL)PHENOL is used as a building block in the synthesis of various organic compounds. Its unique structure and reactivity make it a valuable component in the creation of new molecules with specific properties and applications in different industries.
Used as a Reagent in Chemical Reactions:
4-BROMO-2-(5-ISOXAZOLYL)PHENOL also serves as a reagent in various chemical reactions, facilitating the formation of desired products and enabling the synthesis of complex molecules. Its reactivity and selectivity make it a useful tool in the development of new chemical processes and methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 213690-27-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,6,9 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 213690-27:
(8*2)+(7*1)+(6*3)+(5*6)+(4*9)+(3*0)+(2*2)+(1*7)=118
118 % 10 = 8
So 213690-27-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H6BrNO2/c10-6-1-2-8(12)7(5-6)9-3-4-11-13-9/h1-5,12H

213690-27-8 Well-known Company Product Price

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  • Aldrich

  • (465496)  4-Bromo-2-(5-isoxazolyl)phenol  97%

  • 213690-27-8

  • 465496-5G

  • 968.76CNY

  • Detail

213690-27-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-6-(2H-1,2-oxazol-5-ylidene)cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names Phenol,4-bromo-2-(5-isoxazolyl)

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:213690-27-8 SDS

213690-27-8Downstream Products

213690-27-8Relevant articles and documents

Zn(OTf)2-Catalyzed Formal [3 + 3] Cascade Annulation of Propargylic Alcohols with 2-Aminochromones: Accessing the Chromeno[2,3- b]pyridines

Tong, Pei,Sun, Zhou,Wang, Shutao,Zhang, Yuan,Li, Ying

, p. 13967 - 13974 (2019/10/16)

A Zn(OTf)2-catalyzed formal [3 + 3] cascade annulation strategy for the synthesis of functionalized chromeno[2,3-b]pyridines has been developed using propargylic alcohols and 2-aminochromones as the substrates. The protocol provides a convenien

A Convenient and Practical Synthesis of Aminopyrazoles

Mitchell, David,Luo, Yumei,Mcnulty, Lu Anne M.,Buser, Jonas Y.,Mcfarland, Adam D.

supporting information, p. 235 - 241 (2015/05/05)

A selective methodology for preparing highly substituted aminopyrazoles has been demonstrated. Starting with an acetophenol core, the corresponding substituted isoxazole is prepared in two steps. The isoxazole is transformed into a benzopyran. Alkylation

Synthesis of 2,2′-diaminobischromones using a modified procedure for the rearrangement of 5-(2-hydroxyphenyl)isoxazole to 2-aminochromone

Ghosh, Tarun,Saha, Satyajit,Bandyopadhyay, Chandrakanta

, p. 1845 - 1849 (2007/10/03)

A modified procedure for the rearrangement of 5-(2-hydroxyphenyl)isoxazoles 6a-e to 2-aminochromones 8a-e was developed and this procedure was utilised in the synthesis of hitherto unreported bischromones 3a-c. The isoxazoles 6a-e were prepared regioselec

Synthesis of substituted isoxazoles and 1,3,4-oxadiazoles

Reddy, Kusukuntla Venkat,Sabitha, G.,Subba Rao, A. V.

, p. 697 - 699 (2007/10/03)

A few novel 5-(2'-hydroxyaryl)-isoxazoles 3 and 2-(aryloxymethyl)-3-mercapto-1,3,4-oxadiazoles 8 have been synthesized from the intermediate enamino ketones 2, and tested for their herbicidal activity

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