118486-95-6

Usage

Uses

Used in Organic Synthesis:
5-METHYL-2-(TRIBUTYLSTANNYL)FURAN is used as a reagent in organic synthesis for its ability to participate in cross-coupling reactions, which are essential for the creation of complex organic molecules. The tributylstannyl group attached to the furan ring plays a significant role in these reactions, facilitating the formation of new chemical bonds and contributing to the synthesis of a variety of organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-METHYL-2-(TRIBUTYLSTANNYL)FURAN is used as a precursor in the synthesis of potential drug candidates. Its involvement in cross-coupling reactions allows for the creation of novel molecular structures that may possess therapeutic properties, contributing to the development of new medications.
Used in Chemical Research:
5-METHYL-2-(TRIBUTYLSTANNYL)FURAN is utilized in chemical research as a model compound to study the properties and reactions of organotin compounds and furan derivatives. This helps in understanding the reactivity and potential applications of similar compounds in various chemical processes.
Used in Material Science:
In material science, 5-METHYL-2-(TRIBUTYLSTANNYL)FURAN may be employed in the development of new materials with specific properties. Its participation in cross-coupling reactions can lead to the synthesis of organic compounds that could be used in the creation of advanced materials with applications in various industries, such as electronics, coatings, and polymers.

InChI:InChI=1/C5H5O.3C4H9.Sn/c1-5-3-2-4-6-5;3*1-3-4-2;/h2-3H,1H3;3*1,3-4H2,2H3;/rC17H32OSn/c1-5-8-13-19(14-9-6-2,15-10-7-3)17-12-11-16(4)18-17/h11-12H,5-10,13-15H2,1-4H3

Upstream product

• 534-22-5 2-methylfuran 
• 1461-22-9 tributyltin chloride 

Downstream Products

• 1613270-43-1 N,N'-bis(2,6-diisopropylphenyl)-1,6,9,13-tetra(5-methylfuran-2-yl)terrylene-3,4:11,12-tetracarboxidiimide 
• 400746-82-9 2-(5-methylfuran-2-yl)benzaldehyde 
• 1614251-58-9 1,3-dimethyl-9-(5-methylfuran-2-yl)-5-phenyl-1H-pyrimido[4,5-a]pyrrolizine-2,4(3H,7H)-dione 
• 872025-54-2 (Sp)-8-(5-methyl-2-furyl)-adenosine-2'O-(tert-butyldimethylsilyl)-3',5'-cyclic N-phenylphosphoramidate 
• 108-28-1 protoanemonin 
• 74982-59-5 5-(acetyloxy)-5-methyl-2(5H)-furanone 

Relevant academic research and scientific papers

Adenosine receptor antagonists

The invention provides a compound shown as a formula (I) and a pharmaceutical composition thereof. The compounds of formula (I) of the present invention are useful as adenosine receptor inhibitors, especially A2A and/or A2B inhibitors, for example, the product can be used for prevention or treatment of diseases associated with A2A and/or A2B activity or expression.

Adenosine receptor antagonist

The invention provides a compound shown as a formula (I) and a pharmaceutical composition thereof. The compound of formula (I) of the present invention is useful as adenosine receptor inhibitors, especially A2A and/or A2B inhibitors, for example, in the prevention or treatment of diseases associated with A2A and/or A2B activity or expression.

P2X3 AND/OR P2X2/3 COMPOUNDS AND METHODS

The present application provides novel compounds and methods for preparing and using these compounds. In one embodiment, the compounds are of the structure of formula (I), wherein R1-R4 are defined herein. In a further embodiment, these compounds are useful in method for regulating one or both of the P2X3 or P2X2/3 receptors. In another embodiment, these compounds are useful for treating pain in patients by administering one or more of the compounds to a patient.

TETRACENE DERIVATIVE AND METHOD FOR SYNTHESIZING THE SAME, AND ORGANIC ELECTRONICS DEVICE PREPARED USING THE SAME

PROBLEM TO BE SOLVED: To provide a tetracene derivative having an aromatic heterocycle in a side chain, as a novel compound which can be used as a coating type organic semiconductor material, and a method for synthesizing the same, and an organic electronics device prepared using the same. SOLUTION: This invention provides a tetracene derivative represented by formula (1) (X is O, S, Se or N; and R1 and R2 are H, a linear or branched alkyl group, F, Cl, Br, an alkyl group comprising at least one Br, an aryl group, a heterocycle group, a hydroxy group, an ether group or an amino group. COPYRIGHT: (C)2016,JPO&INPIT

Oxidative Substitution Reactions of Organostannyl Compounds with Lead Tetraacetate. A Convenient Route to 5-Alkylidene-2(5H)-furanones

5-Substituted 2-tributylstannylfurans which were synthesized by the reaction of corresponding 5-substituted 2-lithiofurans with tribitylstannyl chloride, were treated with two equimolar amounts of lead tetraacetate at room temperature to give corresponding 5-substituted 5-acetoxy-2(5H)-furanones in good yields.The 5-acetoxy-2(5H)-furanone was heated at 80 deg C in acetic acid-acetic anhydride containing a catalytic amount of concentrated sulfuric acid to give 5-alkylidene-2(5H)-furanone in moderate yield.