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Isoxazole, 3-(2-furanyl)-5-phenyl-, is a heterocyclic organic compound characterized by a five-membered isoxazole ring fused with a benzene ring and a furan ring. Isoxazole, 3-(2-furanyl)-5-phenyl- is a derivative of isoxazole, which contains a nitrogen atom and an oxygen atom in its structure. The presence of the furan ring at the 3-position and the phenyl ring at the 5-position contributes to its unique chemical properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science. The compound's molecular formula is C12H9NO2, and it has a molecular weight of 199.21 g/mol. Due to its complex structure, it may exhibit various biological activities and chemical reactivity, making it a subject of interest for researchers in organic chemistry and related disciplines.

2976-08-1

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2976-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2976-08-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2976-08:
(6*2)+(5*9)+(4*7)+(3*6)+(2*0)+(1*8)=111
111 % 10 = 1
So 2976-08-1 is a valid CAS Registry Number.

2976-08-1SDS

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-furan-2-yl-5-phenyl-isoxazole

1.2 Other means of identification

Product number -
Other names 3-(

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:2976-08-1 SDS

2976-08-1Relevant academic research and scientific papers

Copper(0) Nanoparticles in Click Chemistry: Synthesis of 3,5-Disubstituted Isoxazoles

Vishwanatha,Sureshbabu, Vommina V.

, p. 1823 - 1833 (2015/02/19)

An efficient procedure for the synthesis of 3,5-disubstituted isoxazoles via [3+2] cycloaddition reaction of in situ generated nitrile oxides with acetylenes employing readily preparable copper(0) nanoparticles is described. A variety of in situ generated

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.

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