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80528-89-8

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80528-89-8 Usage

General Description

29H,31H-Tetrabenzo[b,g,l,q]porphine, 6,13,20,27-tetraphenyl- is a chemical compound that belongs to the porphyrin family. It consists of a porphyrin core with four benzene rings attached at specific positions. This chemical has a unique and complex molecular structure that gives it a wide range of applications, including use as a photosensitizer in photodynamic therapy, as a dye in organic electronics, and as a catalyst in various chemical reactions. Its tetraphenyl substitution also provides enhanced stability and solubility, making it a versatile and valuable compound in multiple fields of research and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 80528-89-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,2 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80528-89:
(7*8)+(6*0)+(5*5)+(4*2)+(3*8)+(2*8)+(1*9)=138
138 % 10 = 8
So 80528-89-8 is a valid CAS Registry Number.

80528-89-8SDS

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 H2TPTBP

1.2 Other means of identification

Product number -
Other names 5,10,15,20-tetraphenyltetrabenzo[b,g,l,q]porphyrin

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:80528-89-8 SDS

80528-89-8Relevant articles and documents

Synthesis, Structural and Optical Properties of Tetrabenzoporphyrin Complexes Bearing Four or Eight Peripheral Phenyl Groups

Furuyama, Taniyuki,Okujima, Tetsuo,Muramatsu, Kota,Takahashi, Yuichi,Mikami, Akihiro,Fukumura, Tomoteru,Mori, Shigeki,Nakae, Takahiro,Takase, Masayoshi,Uno, Hidemitsu,Kobayashi, Nagao

, p. 3224 - 3235 (2019/05/29)

A series of free-base and phosphorus(V) complexes of tetrabenzoporphyrin (TBP) and some phosphorus(V) porphyrins containing four or eight phenyl groups on the periphery have been synthesized and characterized by X-ray crystallography, electronic absorption, and magnetic circular dichroism (MCD) spectroscopy, together with quantum chemical calculations. All phosphorus TBP and meso-tetraphenyl porphyrin complexes adapted ruffled conformations due to the small P(V) ion, although the Zn(II)TBPs containing eight phenyl (Φ) groups at the so-called β and α positions showed planar and saddled structures in the solid state, due to, respectively, marginal or severe steric hindrance between the neighboring Φ groups. All P(V)TBPs showed the Soret and Q bands beyond 450 and 700 nm, respectively, which are some of the longest wavelengths exhibited by metallated TBPs reported to date. Of the eight Φ group-substituted P(V)TBPs, those substituted at α positions always showed absorption bands at longer wavelengths than those at β positions, which was reproduced by calculated absorption spectra. The Soret band positions of meso-tetraphenylated P(V) species without fused benzo-groups (ca. 430–440 nm) were also some of the longest among metalloporphyrins of this type.

Synthesis, electrochemical and spectroelectrochemical characterization of iron(III) tetraarylporphyrins containing four β, β ′-butano and β, β ′-benzo fused rings

Xu, Weijie,Fang, Yuanyuan,Ou, Zhongping,Chen, Mingyuan,Kadish, Karl M.

, p. 521 - 534 (2018/05/14)

Six iron(III) tetraarylporphyrins containing four b,b?-butano or b,b?-benzo fused rings were synthesized and characterized by electrochemistry and spectroelectrochemistry in nonaqueous media. The examined compounds are represented as butano(TpYPP)FeCl and

H2O2-activated triplet-triplet annihilation upconversion via modulation of the fluorescence quantum yields of the triplet acceptor and the triplet-triplet-energy-transfer efficiency

Tao, Renjie,Zhao, Jianzhang,Zhong, Fangfang,Zhang, Caishun,Yang, Wenbo,Xu, Kejing

, p. 12403 - 12406 (2015/08/03)

Oxidation-activatable triplet-triplet annihilation (TTA) upconversion was achieved with 9,10-bis(diphenylphosphino)-anthracene (BDPPA, nonfluorescent) as an activatable triplet acceptor/emitter, which can be oxidized to BDPPA-O (highly fluorescent) by H2O2 under mild conditions, and thus TTA upconversion was switched on by H2O2.

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