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57450-62-1

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57450-62-1 Usage

General Description

5,10,15,20-tetrakis(4-butoxyphenyl)-Porphine, also known as Tetrakis(4-butoxyphenyl)porphyrin (TBP), is a synthetic chemical compound derived from porphyrin. It is a type of porphyrin molecule that contains four butoxyphenyl groups attached to the core structure. TBP is often used as a photosensitizer in photodynamic therapy, a treatment for cancer and other diseases that involves using light to activate a photosensitive drug. Additionally, TBP has also been studied for its potential applications in organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), due to its unique optical and electronic properties. Its chemical structure and properties make it a valuable tool for various medical and technological applications.

Check Digit Verification of cas no

The CAS Registry Mumber 57450-62-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,5 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57450-62:
(7*5)+(6*7)+(5*4)+(4*5)+(3*0)+(2*6)+(1*2)=131
131 % 10 = 1
So 57450-62-1 is a valid CAS Registry Number.
InChI:InChI=1/C60H62N4O4/c1-5-9-37-65-45-21-13-41(14-22-45)57-49-29-31-51(61-49)58(42-15-23-46(24-16-42)66-38-10-6-2)53-33-35-55(63-53)60(44-19-27-48(28-20-44)68-40-12-8-4)56-36-34-54(64-56)59(52-32-30-50(57)62-52)43-17-25-47(26-18-43)67-39-11-7-3/h13-36,61,64H,5-12,37-40H2,1-4H3/b57-49-,57-50-,58-51-,58-53-,59-52-,59-54-,60-55-,60-56-

57450-62-1SDS

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 5,10,15,20-tetrakis(4-butoxyphenyl)-21,22-dihydroporphyrin

1.2 Other means of identification

Product number -
Other names 5,10,15,20-tetrakis-(4-butoxy-phenyl)-21H,23H-porphine

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:57450-62-1 SDS

57450-62-1Downstream Products

57450-62-1Relevant articles and documents

Side chain modified porphyrin molecules and application thereof

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Paragraph 0061; 0065; 0067, (2019/12/25)

The invention discloses side chain modified porphyrin molecules and application thereof. According to the side chain modified porphyrin molecules, porphyrin molecules with electron enriching functionsare adopted as a core of capturing charges, an alkoxy chain segment is adopted as an inhibition part of a charge transfer process, and the molecules are ensured to be applied to flexible structures for solution processing. Molecule structures are reasonably designed from the view of film morphologies, preparation processes and performance regulation and control, and properties of organic field effect transistor storage devices are compared. The invention provides a material and device preparation method which is feasible in commercial popularization, low in cost and simple in process while properties of storage devices are regulated.

SYNTHESIS, EQUILIBRIUM SOLUBILITY, AND ELECTRONIC AND PMR SPECTRA OF meso-TETRA(ALKOXYPHENYL)PORPHYRINES

Semeikin, A. S.,Koifman, O. I.,Nikitina, G. E.,Berezin, B. D.

, p. 1423 - 1426 (2007/10/02)

Tetra(alkoxyphenyl)porphines, readily soluble in nonpolar solvents, were synthesized from tetra(hydroxyphenyl)porphines.The equilibrium solubility was determined in hexane at 25 deg C, and its relation to the number of carbon atoms in the alkyl chain has

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