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3-(tert-butyl)-1-methylnaphthalene is an organic compound with the molecular formula C15H18. It is a derivative of naphthalene, a bicyclic aromatic hydrocarbon, with a tert-butyl group attached to the 3-position and a methyl group at the 1-position. 3-(tert-butyl)-1-methylnaphthalene is characterized by its unique structure, which contributes to its specific chemical properties and potential applications. It is often used as a precursor in the synthesis of various organic compounds and can be found in research and industrial settings. Due to its complex structure, 3-(tert-butyl)-1-methylnaphthalene may have specific solubility, reactivity, and stability characteristics that make it suitable for certain chemical reactions and processes.

883-80-7

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883-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 883-80-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,8 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 883-80:
(5*8)+(4*8)+(3*3)+(2*8)+(1*0)=97
97 % 10 = 7
So 883-80-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H18/c1-11-9-13(15(2,3)4)10-12-7-5-6-8-14(11)12/h5-10H,1-4H3

883-80-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-tert-butyl-1-methylnaphthalene

1.2 Other means of identification

Product number -
Other names 1-Methyl-3-tert.butyl-naphthalin

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 -
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More Details:883-80-7 SDS

883-80-7Downstream Products

883-80-7Relevant academic research and scientific papers

Electron Paramagnetic Resonance Spectra of Substituted 1- and 2-Naphthylmethyl Radicals

Jackson, Richard A.,Rhodes, Christopher J.

, p. 53 - 57 (2007/10/02)

The EPR spectra of 7-tert-butyl-1-naphthylmethyl and 6-tert-butyl-2-naphthylmethyl radicals, prepared by photolysis of the hydrocarbon with tert-butyl peroxide at -40 deg C, have been analysed by correlation methods: average α(C-H) coupling constants are 15.0 and 15.25 G respectively, in line with the expected relative stabilities of the two radicals and the recently reported stabilization energy for 1-naphthylmethyl.

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