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6-(1-phenylethyl)-1,2,3,4-tetrahydronaphthalene is a complex organic compound with the molecular formula C18H20. It is a derivative of naphthalene, a bicyclic aromatic hydrocarbon, with a phenylethyl group attached to the 6th carbon atom. The compound is characterized by its unique structure, which consists of a naphthalene ring fused to a tetrahydro ring, and a phenylethyl side chain. This chemical is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its versatile chemical properties and potential for further functionalization. Its stability, reactivity, and solubility in organic solvents make it a valuable intermediate in the development of new chemical entities.

6196-98-1

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6196-98-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6196-98-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,9 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6196-98:
(6*6)+(5*1)+(4*9)+(3*6)+(2*9)+(1*8)=121
121 % 10 = 1
So 6196-98-1 is a valid CAS Registry Number.

6196-98-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(1-phenyl-ethyl)-1,2,3,4-tetrahydro-naphthalene

1.2 Other means of identification

Product number -
Other names 6-(1-PHENYLETHYL)-1,2,3,4-TETRAHYDRONAPHTHALENE

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:6196-98-1 SDS

6196-98-1Downstream Products

6196-98-1Relevant academic research and scientific papers

A novel InCl3/SiO2-catalyzed hydroarylation of arenes with styrenes under solvent-free conditions

Sun, Gaojun,Sun, Huayin,Wang, Zhiyong,Zhou, Ming-Ming

experimental part, p. 1096 - 1100 (2009/04/04)

A novel InCl3/SiO2-catalyzed hydroarylation of various styrenes with arenes has been developed. The reaction can be carried out under solvent-free conditions to afford a series of 1,1-diarylalkanes in high yields and with good regioselectivities. The catalyst can be reused six times without obvious loss of catalytic activity. Georg Thieme Verlag Stuttgart.

THERMAL TRANSFER FLUID: 1-PHENYL-1-TETRAHYDRONAPHTHYLETHANE.

Matsumoto,Furukawa,Tanaka,Yano,Kamita

, p. 215 - 218 (2007/10/14)

Naphthalene was selectively hydrogenated to tetralin, followed by reaction with styrene to give 1-phenyl-1-tetrahydronaphthylethane in 87% yield. Efficient catalysts for the reaction were 90% sulfuric acid or solid acids possessing acid sites of H//0 less than or equal to minus 5. 6. Purified 1-phenyl-1-tetrahydronaphthylethane has favored properties for a high boiling point thermal transfer fluid: boiling point, 342 C; pour point minus 37. 5 C; good thermal stability, etc. On severe heating, it decomposed to low fractions to some extent with little tendency to polymerization.

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