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13484-04-3

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13484-04-3 Usage

Description

3-(4-Bromophenyl)isoxazole, also known as 4-Bromo-3-phenylisoxazole, is a heterocyclic chemical compound with the molecular formula C9H6BrNO. It features a five-membered ring containing oxygen and nitrogen atoms, with a bromine atom attached to a phenyl group. This versatile intermediate is widely used in organic synthesis and pharmaceutical research.

Uses

Used in Organic Synthesis:
3-(4-Bromophenyl)isoxazole is used as a building block in organic synthesis for the creation of various biologically active molecules. Its unique structure allows for the formation of diverse chemical compounds, making it a valuable component in the development of new organic materials.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3-(4-Bromophenyl)isoxazole serves as a scaffold for potential drug candidates. Its chemical properties and structural features make it a promising candidate for the design and synthesis of novel therapeutic agents.
Used as a Ligand in Coordination Chemistry:
3-(4-Bromophenyl)isoxazole is also utilized as a ligand in coordination chemistry. Its ability to form stable complexes with metal ions contributes to the development of new coordination compounds with potential applications in various fields, such as catalysis, materials science, and medicinal chemistry.
Overall, 3-(4-Bromophenyl)isoxazole is a versatile intermediate with significant potential for use in the chemical and pharmaceutical industries, playing a crucial role in the synthesis of biologically active molecules and the development of new pharmaceutical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 13484-04-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,8 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13484-04:
(7*1)+(6*3)+(5*4)+(4*8)+(3*4)+(2*0)+(1*4)=93
93 % 10 = 3
So 13484-04-3 is a valid CAS Registry Number.

13484-04-3 Well-known Company Product Price

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  • Aldrich

  • (697028)  3-(4-Bromophenyl)isoxazole  97%

  • 13484-04-3

  • 697028-1G

  • 1,601.73CNY

  • Detail

13484-04-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-bromophenyl)-1,2-oxazole

1.2 Other means of identification

Product number -
Other names 3-(4-Brom-phenyl)-isoxazol

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:13484-04-3 SDS

13484-04-3Relevant articles and documents

Preparation method of isoxazole derivative

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Paragraph 0060-0065, (2019/12/02)

The invention relates to a preparation method of an isoxazole derivative, which comprises the following steps of mixing an propargyl alcohol derivative, a halogen source, an acid and a solvent, and heating to react; adding the hydroxylamine into the react

Efficient and regioselective one-pot synthesis of 3-substituted and 3,5-disubstituted isoxazoles

Tang, Shibing,He, Jinmei,Sun, Yongquan,He, Liuer,She, Xuegong

supporting information; experimental part, p. 3982 - 3985 (2009/12/03)

(Figure Presented) A series of 3-substituted and 3,5-disubstituted isoxazoles have been efficiently synthesized in moderate to excellent yields by the reaction of N-hydroxyl-4-toluenesulfonamide with α,β-unsaturated aldehydes/ketones. This novel strategy is associated with readily available starting materials, mild conditions, high regioselectivity, and wide scope.

Synthesis of azirines containing aldehyde functionality and their utilization as synthetic tools for five membered oxazoles and isoxazoles

Brahma, Sulagna,Ray, Jayanta K.

, p. 311 - 317 (2008/09/20)

(Chemical Equation Presented) A simple and useful procedure for the synthesis of azirines containing aldehyde functionality from open chain bromo/chloro-aldehydes at room temperature is reported. The scope of the ring expansion reaction of a number of 3-s

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