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1-(3-Ethoxyoct-1-ynyl)benzene is an organic compound characterized by a unique molecular structure. It consists of a benzene ring (C6H5) attached to a 3-ethoxyoct-1-ynyl group, which is an alkyne chain with an ethoxy group (C2H5O) at the third carbon position. The compound is represented by the formula C16H22O, indicating 16 carbon atoms, 22 hydrogen atoms, and 1 oxygen atom. This chemical is primarily used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its properties include a low melting point, low toxicity, and good solubility in organic solvents. Due to its versatile structure, 1-(3-ethoxyoct-1-ynyl)benzene can be further functionalized and modified to create a wide range of derivatives with diverse applications in the chemical industry.

1902-94-9

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1902-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1902-94-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,0 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1902-94:
(6*1)+(5*9)+(4*0)+(3*2)+(2*9)+(1*4)=79
79 % 10 = 9
So 1902-94-9 is a valid CAS Registry Number.

1902-94-9Relevant academic research and scientific papers

Nucleophilic substitution of secondary alkyl-substituted propargyl acetates: An economic and practical indium trichloride catalyzed access

Lin, Min,Hao, Lu,Liu, Xiao-Tao,Chen, Qing-Zhen,Wu, Feng,Yan, Ping,Xu, Su-Xia,Chen, Xin-Liang,Wen, Jia-Jie,Zhan, Zhuang-Ping

scheme or table, p. 665 - 670 (2011/04/26)

An economic and practical transformation from secondary alkyl-substituted propargyl acetates to a variety of nucleophilic substitution products was described. This reaction was catalyzed by inexpensive InCl3. High yields and excellent chemosele

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