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Methanone, [5-[[3-(4-iodophenyl)-1H-pyrrol-2-yl]methyl]-1H-pyrrol-2-yl](4-methylphen yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

312260-64-3

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312260-64-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 312260-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,2,2,6 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 312260-64:
(8*3)+(7*1)+(6*2)+(5*2)+(4*6)+(3*0)+(2*6)+(1*4)=93
93 % 10 = 3
So 312260-64-3 is a valid CAS Registry Number.

312260-64-3Relevant academic research and scientific papers

Rational synthesis of β-substituted chlorin building blocks

Balasubramanian,Strachan,Boyle,Lindsey

, p. 7919 - 7929 (2007/10/03)

Chlorins bearing synthetic handles at specific sites about the perimeter of the macrocycle constitute valuable building blocks. We previously developed methodology for preparing meso-substituted chlorin building blocks and now present methodology for preparing several complementary β-substituted chlorin building blocks. The chlorins bear one or two β substituents, one meso substituent, a geminal dimethyl group to lock in the chlorin hydrogenation level, and no flanking meso and β substituents. The synthesis involves convergent joining of an Eastern half and a Western half. New routes have been developed to two β-substituted bromo-dipyrromethane monocarbinols (Eastern halves). A new β-substituted Western half was prepared following the method for preparing an unsubstituted Western half (3,3-dimethyl-2,3-dihydrodipyrrin). Chlorin formation is achieved by a two-flask process of acid-catalyzed condensation followed by metal-mediated oxidative cyclization, β-Substituted chlorins have been prepared in 18-24% yield bearing a 4-iodophenyl group at the 8-position, a 4-iodophenyl group or a 4-[2-(trimethylsilyl)ethynyl]phenyl group at the 12-position, and a 4-iodophenyl group and a 4-[2-(trimethylsilyl)ethynyl]phenyl group at diametrically opposed β-positions (2, 12). The latter building block makes possible the stepwise construction of linear multi-chlorin architectures. The chlorins exhibit typical absorption and fluorescence spectra. A systematic shift in the absorption maximum (637-655 nm for the free base chlorins, 606-628 nm for the zinc chlorins) and intensity of the chlorin Q(y) band (ε up to 79 000 M-1 cm-1) is observed depending on the location of the substituents. The characteristic spectral features and location of substituents in defined positions make these chlorins well suited for a variety of applications in biomimetic and materials chemistry.

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