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91569-62-9

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91569-62-9 Usage

Type of compound

Nitronaphthalene derivative

Functional groups

Ethoxy group, Nitro group

Classification

Nitroaromatic compound

Common use

Solvent

Industrial applications

a. Synthesis of pharmaceuticals
b. Dye intermediate
c. Chemical intermediate for organic reactions

Safety considerations

Handle with care and follow safety guidelines for use and disposal

Check Digit Verification of cas no

The CAS Registry Mumber 91569-62-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,6 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 91569-62:
(7*9)+(6*1)+(5*5)+(4*6)+(3*9)+(2*6)+(1*2)=159
159 % 10 = 9
So 91569-62-9 is a valid CAS Registry Number.

91569-62-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethoxy-4-nitronaphthalene

1.2 Other means of identification

Product number -
Other names ethyl-(4-nitro-[1]naphthyl)-ether

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:91569-62-9 SDS

91569-62-9Relevant articles and documents

Synthesis of 1-alkoxy-4-nitronaphthalenes in a novel nitration of naphthalene

Mellor, John M.,Parkes, Rachel,Millar, Ross W.

, p. 8739 - 8742 (2007/10/03)

A new nitration of naphthalene affords as major products 1,4-disubstituted naphthalenes and as minor products 12-disubstituted naphthalenes. By use of eerie ammonium nitrate suspended on silica gel, or in homogeneous solution, nitration of naphthalene in the presence of alcohols, sodium- or tetrabutyl ammonium- nitrite and acid gives alkoxynitronaphthalenes. A preparation of 1-nitroaaphthalene is described under heterogeneous conditions.

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