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Naphthalene, 1,2,3,4-tetrahydro-6-(4-phenylbutyl)-, also known as 1,2,3,4-tetrahydro-6-(4-phenylbutyl)naphthalene, is an organic compound with the molecular formula C20H24. It is a derivative of naphthalene, a polycyclic aromatic hydrocarbon, with a four-carbon chain (butyl) attached to the 6th carbon and a phenyl group attached to the 4th carbon of the butyl chain. Naphthalene, 1,2,3,4-tetrahydro-6-(4-phenylbutyl)- is characterized by its unique structure, which contributes to its specific chemical properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science. Due to its complex structure, it is essential to handle Naphthalene, 1,2,3,4-tetrahydro-6-(4-phenylbutyl)- with care and follow proper safety guidelines during its synthesis, storage, and use.

5509-23-9

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5509-23-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5509-23-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,0 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5509-23:
(6*5)+(5*5)+(4*0)+(3*9)+(2*2)+(1*3)=89
89 % 10 = 9
So 5509-23-9 is a valid CAS Registry Number.

5509-23-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(4-phenylbutyl)-1,2,3,4-tetrahydronaphthalene

1.2 Other means of identification

Product number -
Other names 1-Phenyl-4-(1,2,3,4-tetrahydro-[6]naphthyl)-butan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5509-23-9 SDS

5509-23-9Upstream product

5509-23-9Relevant 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 (2007/10/02)

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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