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80588-48-3

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80588-48-3 Usage

General Description

1,3,4,5,6,7,8-heptafluoro-N-(pentafluorophenyl)naphthalen-2-amine is a chemical compound with the molecular formula C16H3F13N. It is a member of the amine class of compounds and contains a heptafluoro substitution on the naphthalene ring, as well as a pentafluorophenyl group. 1,3,4,5,6,7,8-heptafluoro-N-(pentafluorophenyl)naphthalen-2-amine is a fluorinated amine with multiple fluorine atoms attached to the naphthalene ring and is used in various chemical and pharmaceutical applications. It is known for its high stability and potentially useful properties in pharmaceutical research, as well as other industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 80588-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,8 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80588-48:
(7*8)+(6*0)+(5*5)+(4*8)+(3*8)+(2*4)+(1*8)=153
153 % 10 = 3
So 80588-48-3 is a valid CAS Registry Number.

80588-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,4,5,6,7,8-heptafluoro-N-(2,3,4,5,6-pentafluorophenyl)naphthalen-2-amine

1.2 Other means of identification

Product number -
Other names -

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:80588-48-3 SDS

80588-48-3Downstream Products

80588-48-3Relevant articles and documents

POLYFLUORO-ARYL CONTAINING N-ANIONS AND THE 1H AND 19F NMR SPECTRA OF THEIR SALTS

Vlasov, V. M.,Yakobson, G. G.

, p. 1955 - 1963 (2007/10/02)

The salts of N-anions of types Na and Na were generated by the reaction of sodium hydride with polyfluoroaryl-containing NH acids (polyfluoroaryl- and diarylamines, polyfluorobenzanilides, polyfluoroacetanilides) in 1,2-dimethoxyethane.Satisfactory linear correlations are observed between the parameters of the 1H and 19F NMR spectra of solutions of the salts of the N anions and NH acids and also the ? constants of the substituents R.From comparison of the chemical shifts of the para-fluorine atom in the salts of the ambient N-anions and the structurally similar enolate anions it follows that the increase in the interaction of the C6F5 group with negative charge in the ? system in the N-anions is due to the greater localization of charge on the nitrogen atom in the latter than on the carbon atom in the enolate anions.

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