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2388-43-4

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2388-43-4 Usage

Structure

Naphthalene derivative with a methoxy group at the 1-position and a naphthalen-1-ylmethyl group at the 4-position

Usage

Fluorescent dye, chemical intermediate, fluorescent probe in research laboratories, potential applications in the development of new materials for optical and electronic devices

Safety

Potential health and safety hazards, proper handling and disposal procedures should be followed.

Check Digit Verification of cas no

The CAS Registry Mumber 2388-43-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2388-43:
(6*2)+(5*3)+(4*8)+(3*8)+(2*4)+(1*3)=94
94 % 10 = 4
So 2388-43-4 is a valid CAS Registry Number.

2388-43-4SDS

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 1-methoxy-4-[(4-methoxynaphthalen-1-yl)methyl]naphthalene

1.2 Other means of identification

Product number -
Other names Bis(4-methoxynaphthalen-1-yl)methane

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:2388-43-4 SDS

2388-43-4Downstream Products

2388-43-4Relevant articles and documents

Syntheses of Calixnaphthalenes Derived from 1-Naphthol

Georghiou, Paris E.,Ashram, Muhammad,Li, Zhaopeng,Chaulk, Steven G.

, p. 7284 - 7289 (1995)

Using a convergent synthetic strategy, the synthesis of the previously elusive C4ν-symmetrical calixnaphthalene from 1-naphthol is described.Using other independent convergent routes, syntheses of the other three isomeric calixnaphthalenes originally formed from the direct base-catalyzed condensation of formaldehyde with 1-naphthol are also described.All of these methods involved either a TiCl4- or TFA-assisted coupling reaction to achieve the cyclization steps.A mechanism is proposed to account for the formation of the original three isomeric calixnaphthalenes from the base-catalyzed condensation of formaldehyde with 1-naphthol.

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