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6502-18-7

1-(but-3-yn-1-yl)-2-methylbenzene, also known as 2-methyl-1-(3-butyn-1-yl)benzene, is an organic compound with the molecular formula C11H12. It is a derivative of benzene, featuring a methyl group at the 2nd carbon position and a but-3-yn-1-yl group attached to the 1st carbon position. 1-(but-3-yn-1-yl)-2-methylbenzene is characterized by its unique structure, which includes a triple bond in the but-3-yn-1-yl group, providing it with distinct chemical properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science. The compound's structure and properties make it a versatile building block for the synthesis of more complex molecules and a subject of interest in organic chemistry research.

6502-18-7

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6502-18-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6502-18-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,0 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6502-18:
(6*6)+(5*5)+(4*0)+(3*2)+(2*1)+(1*8)=77
77 % 10 = 7
So 6502-18-7 is a valid CAS Registry Number.

6502-18-7Relevant articles and documents

Superoxide mediated isomerization of 4-aryl-but-1-ynes to 1-aryl-1,3-butadienes

Khan, Faiz Ahmed,Budanur, Basavaraj M.

, p. 7600 - 7607 (2015)

A new role of superoxide ion in the isomerization of homobenzylic acetylenes leading to 1-aryl-1,3-butadienes is reported. The unconventional reagent KO2 is found to be superior in performing this kind of isomerization over other the commonly u

Metal-Free Synthesis of Selenodihydronaphthalenes by Selenoxide-Mediated Electrophilic Cyclization of Alkynes

An, Shaoyu,Li, Pingfan,Zhang, Zhong

, p. 3059 - 3070 (2021/07/22)

A transition-metal-free, selenium mediated electrophilic cyclization reaction was realized through a one-pot procedure between simple alkynes and triflic anhydride-activated selenoxides to give selenium containing dihydronaphthalene products. This method gave good to very high yields for all products, including selenium-substituted phenanthrene, dihydroquinoline, 2H-chromene, and coumarin, which can be further transformed to other functionalized compounds.

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