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Naphthalene, 2,2'-(1,4-butanediyl)bis[5,6,7,8-tetrahydro-] is a complex organic compound with the chemical formula C18H22. It is a derivative of naphthalene, which is a polycyclic aromatic hydrocarbon consisting of two fused benzene rings. The compound is characterized by the presence of a 1,4-butanediyl bridge connecting two tetrahydro-naphthalene units. Tetrahydro-naphthalene refers to the partially hydrogenated form of naphthalene, where four hydrogen atoms have been added to the molecule, reducing its aromaticity. This specific compound is known for its potential applications in various chemical industries, such as in the synthesis of pharmaceuticals, dyes, and other organic compounds. Due to its complex structure, it is important to handle Naphthalene, 2,2'-(1,4-butanediyl)bis[5,6,7,8-tetrahydro- with care, as it may have specific safety and environmental considerations.

1914-37-0

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1914-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1914-37-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,1 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1914-37:
(6*1)+(5*9)+(4*1)+(3*4)+(2*3)+(1*7)=80
80 % 10 = 0
So 1914-37-0 is a valid CAS Registry Number.

1914-37-0Upstream product

1914-37-0Downstream Products

1914-37-0Relevant academic research and scientific papers

Formation of 6,6'-(Butane-1,4-diyl)bis(1,2,3,4-tetrahydronaphthalene) in the Reaction of Tetralin with Aluminium Chloride

Wilson, Michael A.,Rottendorf, Horst,Collin, Philip J.,Vasallo, Anthony M.

, p. 2379 - 2383 (1984)

It has been shown that the reaction of aluminium chloride with tetralin yields 6,6'-(butane-1,4-diyl)-bis(1,2,3,4-tetrahydronaphthalene) as well as a number of other products.It is suggested that this compound is formed by protonation of tetralin, fragmentation of the alicyclic ring and then electrophilic attack of a further tetralin molecule.The positions of substitution in the product suggests that ion pairs are involved in the reaction.It is clear that intermediates have sufficient lifetime to undergo intermolecular substitution reactions in addition to intramolecular substitution or proton loss.

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