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19491-17-9

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19491-17-9 Usage

Chemical structure

1,1'-Binaphthalene, 2,2'-diethoxy-
It consists of two naphthalene rings connected by a single bond, with two ethoxy (C2H5O) groups attached to each of the naphthalene rings.

Derivative

Binaphthalene
1,1'-Binaphthalene, 2,2'-diethoxyis derived from binaphthalene, a compound consisting of two naphthalene rings fused together.

Chiral ligand

Asymmetric catalysis
The compound is commonly used in organic synthesis as a chiral ligand, which helps in the selective formation of one enantiomer over the other in asymmetric catalysis.

Applications

Different sources of media describe the Applications of 19491-17-9 differently. You can refer to the following data:
1. Pharmaceutical and agrochemical production
It is used in the production of pharmaceuticals and agrochemicals due to its ability to influence the stereochemistry of the synthesized compounds.
2. Liquid crystals and dyes
The compound is also used in the production of liquid crystals and dyes, taking advantage of its unique structural and electronic properties.

Potential applications

Materials science and optoelectronics
Due to its unique structural and electronic properties, 1,1'-Binaphthalene, 2,2'-diethoxyhas potential applications in the fields of materials science and optoelectronics.

Physical state

Likely a solid at room temperature
Although not explicitly mentioned, most organic compounds with a molecular weight of around 366 g/mol (C26H26O2) are solids at room temperature.

Solubility

Likely soluble in organic solvents
Given its nonpolar nature and the presence of carbon-hydrogen bonds, the compound is likely soluble in organic solvents such as dichloromethane, ethyl acetate, or toluene.

Stability

Stable under normal conditions
As a general rule, organic compounds with single bonds and no highly reactive functional groups are stable under normal conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 19491-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,9 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19491-17:
(7*1)+(6*9)+(5*4)+(4*9)+(3*1)+(2*1)+(1*7)=129
129 % 10 = 9
So 19491-17-9 is a valid CAS Registry Number.

19491-17-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethoxy-1-(2-ethoxynaphthalen-1-yl)naphthalene

1.2 Other means of identification

Product number -
Other names 2,2'-Diaethoxy-[1,1']binaphthyl

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:19491-17-9 SDS

19491-17-9Upstream product

19491-17-9Relevant articles and documents

Regioselective Halogenation and Dimerization of Alkoxynaphathalenes with Alumina- or Kieselguhr-supported Copper(II) Halides

Suzuki, Yoshitada,Takeuchi, Kiyoshi,Kodomari, Mitsuo

, p. 426 - 427 (2007/10/03)

The reaction of 1-alkoxynaphathalenes 1 with alumina-supported copper(II) bromide or copper(II) chloride gave dimers, 4,4'-dialkoxy-1,1'-binaphthyls 3, as major products, and with Kieselguhr-supported copper(II) bromide afforded 1-bromo-4-alkoxynaphthalenes 2, while the reaction of 2-alkoxynaphathalenes 4 with alumina- or Kieselguhr-supported copper(II) bromide gave preferentially 1-bromo-2-alkoxynaphthalenes 5.

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