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32562-61-1

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32562-61-1 Usage

General Description

Hematoporphyrin IX dimethylester is a synthetic compound derived from hematoporphyrin, and is used in photodynamic therapy for the treatment of various cancers and other medical conditions. It is a photosensitizer that becomes activated by light of a specific wavelength, leading to the production of reactive oxygen species that can destroy targeted cells. This mechanism of action makes it particularly effective in destroying cancer cells while sparing healthy tissues. Hematoporphyrin IX dimethylester is also being investigated for its potential in imaging and diagnostics, and is considered a promising tool in the field of medical oncology.

Check Digit Verification of cas no

The CAS Registry Mumber 32562-61-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,5,6 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 32562-61:
(7*3)+(6*2)+(5*5)+(4*6)+(3*2)+(2*6)+(1*1)=101
101 % 10 = 1
So 32562-61-1 is a valid CAS Registry Number.

32562-61-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-[8,13-bis(1-hydroxyethyl)-18-(3-methoxy-3-oxopropyl)-3,7,12,17-tetramethyl-22,23-dihydroporphyrin-2-yl]propanoate

1.2 Other means of identification

Product number -
Other names haematoporphyrin dimethyl ester

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:32562-61-1 SDS

32562-61-1Relevant articles and documents

Isomeric monoacetylmono(1-hydroxyethyl)deuteroporphyrins: Syntheses, characterization, and use for the syntheses of regioselectively methyl- and vinyl-deuterated hemins

Shiau,Pandey,Ramaprasad,Dougherty,Smith

, p. 2190 - 2195 (1990)

Treatment of hematoporphyrin IX dimethyl ester (7) with tetrapropylammonium perruthenate (Pr(n)4N(RuO4) and N-methylmorpholine N-oxide affords a high yield of the separable monoacetylmono(1-hydroxyethyl)-deuteroporphyrin isomers 5 and 6. Proton NMR NOE experiments and chemical transformations involving specific individual deuteration at the 1- and 3-methyls and 2- and 4-vinyls are used to characterize the isomers.

Process For Preparing Porphyrin Derivatives, Such As Protoporphyrin (IX) And Synthesis Intermediates

-

Page/Page column 13; 20, (2008/12/07)

The present invention relates to a process for preparing a porphyrin of formula (I), optionally in the form of a salt with an alkali metal and/or in the form of a metal complex: in which: R and R′ are as defined in claim 1, comprising: a step of condensation, in an acidic medium, between a dipyrromethane of formula (II): in which R′b is as defined above for (I), and a dipyrromethane of formula (III): in which R″ is as defined in claim 1, and also the compounds of formula (III).

A FACILE PORPHYRIN ESTERIFICATION / ETHERIFICATION PROCEDURE

Byrne, Christopher J.,Ward, A. David

, p. 1421 - 1424 (2007/10/02)

Porphyrin carboxylic acids and 1-hydroxyethyl groups can be rapidly esterified and etherified using alcohol/trialkyl orthoformate/strong acid mixtures; addition of water to the reagent permits esterification only.

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