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5441-28-1

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5441-28-1 Usage

Appearance

White to off-white powder

Melting point

224-226°C

Organic electronics

Thin-film transistor material for electronic devices

Antimicrobial properties

Investigated for its ability to inhibit the growth of microorganisms

Antioxidant properties

Studied for its potential to neutralize harmful free radicals

Synthesis

Used as a building block in the synthesis of other organic compounds

Research areas

Pharmaceutical and material science

Structure

Contains a phthalazine core with two 4-methoxyphenyl groups attached to the 1 and 4 positions

Check Digit Verification of cas no

The CAS Registry Mumber 5441-28-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5441-28:
(6*5)+(5*4)+(4*4)+(3*1)+(2*2)+(1*8)=81
81 % 10 = 1
So 5441-28-1 is a valid CAS Registry Number.
InChI:InChI=1/C22H18N2O2/c1-25-17-11-7-15(8-12-17)21-19-5-3-4-6-20(19)22(24-23-21)16-9-13-18(26-2)14-10-16/h3-14H,1-2H3

5441-28-1SDS

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 1,4-bis(4-methoxyphenyl)phthalazine

1.2 Other means of identification

Product number -
Other names 1,4-bis-(4-methoxy-phenyl)-phthalazine

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:5441-28-1 SDS

5441-28-1Downstream Products

5441-28-1Relevant articles and documents

1. 4 - (hydroxy-phenyl) II - 2, 3 - naphthyridine derivatives and their synthetic method

-

, (2017/08/25)

The invention discloses 1,4-di(para hydroxybenzene) based-2,3-quinazoline and a synthesis method thereof. In the synthesis method, a Grignard reagent is prepared from para-halogen anisole and magnesium ribbons and is reacted with phthalic anhydride in a tetrahydrofuran/toluene, 2-methyl tetrahydrofuran/toluene, or diethyl ether/toluene mixing solvent to obtain benzol-1,2-di(para-methoxyl)benzophenone; under the solvent of glacial acetic acid or alcohol, the benzol-1,2-bi(para-methoxyl)benzophenone is reacted again with hydrazine hydrate to obtain 2,3-quinazoline1,4-bi-hydroxybenzene; and finally the 2,3-quinazoline1,4-bi-hydroxybenzene is demethylated under the participation of 40 percent of hydrobromic acid by taking the glacial acetic acid as the solvent to obtain the product. The invention provides a new monomer for developing a high-property polymer material with a quinazoline structure. The invention has reasonable and simple selection for a technical route as well as convenience and easy operation and provides a successful synthesis method for the synthesis of the intermediate of the high polymer product technically.

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