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5,10,15,20-tetrakis(4-octadecyloxyphenyl)-21H,23H-porphyrin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88367-40-2

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88367-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88367-40-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,6 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88367-40:
(7*8)+(6*8)+(5*3)+(4*6)+(3*7)+(2*4)+(1*0)=172
172 % 10 = 2
So 88367-40-2 is a valid CAS Registry Number.

88367-40-2Downstream Products

88367-40-2Relevant academic research and scientific papers

Self-assembly of covalently linked porphyrin dimers at the solid-liquid interface

Habets, Thomas,Lensen, Dennis,Speller, Sylvia,Elemans, Johannes A.A.W.

, (2019)

The synthesis and surface self-assembly behavior of two types of metal-porphyrin dimers is described. The first dimer type consists of two porphyrins linked via a rigid conjugated spacer, and the second type has an alkyne linker, which allows rotation of

Side chain modified porphyrin molecules and application thereof

-

Paragraph 0075; 0079; 0081, (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 of some New Tetra-arylporphyrins for Studies in Solar Energy Conversion

Milgrom, Lionel R.

, p. 2535 - 2539 (2007/10/02)

The synthesis of tetra-arylporphyrins, for studies in solar energy conversion, is described.They are derived from 5,10,15,20-meso-tetrakis(4-hydroxyphenyl)porphyrin (4) which, in basic media, forms a green intermediate that is probably the tetraphenoxide

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