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2,2,5,5-Tetraphenyl-3-hexyne is an organic compound characterized by its unique molecular structure, which consists of a hexyne backbone with four phenyl groups attached. 2,2,5,5-tetraphenyl-3-hexyne is classified as an alkyne due to the presence of a carbon-carbon triple bond, which is located between the second and third carbon atoms in the hexyne chain. The four phenyl groups are symmetrically attached to the terminal carbons of the hexyne, contributing to the compound's stability and unique physical properties. 2,2,5,5-Tetraphenyl-3-hexyne is primarily used in chemical research and as a precursor in the synthesis of more complex organic molecules. Its chemical formula is C30H24, and it has a molecular weight of 384.5 g/mol. The compound is known for its low reactivity due to the electron-donating nature of the phenyl groups, which can stabilize the molecule and reduce the reactivity of the triple bond.

1483-63-2

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1483-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1483-63-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1483-63:
(6*1)+(5*4)+(4*8)+(3*3)+(2*6)+(1*3)=82
82 % 10 = 2
So 1483-63-2 is a valid CAS Registry Number.

1483-63-2Downstream Products

1483-63-2Relevant academic research and scientific papers

Formation and rearrangement of gem-dilithiodiphenylethene

Maercker, Adalbert,Boes, Benno,Hajgholipour, Mohammad Taghi

, p. 143 - 149 (2007/10/03)

1,1-Dilithio-2,2-diphenylethene (14) is accessible through double bromine lithium exchange reaction starting from 1,1-dibromo-2,2-diphenylethene (5) with lithium metal at -110°C. 14 undergoes rearrangement into (E)-1-lithio-2-(2-lithiophenyl)-2-phenylethene (13) at temperatures above -100°C. The (Z)-compound 15 was formed from the (E)-compound 13 at temperatures above -25°C.

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