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meso-(2-bromophenyl)dipyrromethane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

191997-22-5

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191997-22-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 191997-22-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,9,9 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 191997-22:
(8*1)+(7*9)+(6*1)+(5*9)+(4*9)+(3*7)+(2*2)+(1*2)=185
185 % 10 = 5
So 191997-22-5 is a valid CAS Registry Number.

191997-22-5Relevant academic research and scientific papers

K2S2O8mediated synthesis of 5-Aryldipyrromethanes and meso-substituted A4-Tetraarylporphyrins

Laha, Joydev K.,Hunjan, Mandeep Kaur

, p. 664 - 673 (2021/06/03)

The synthesis of dipyrromethanes from pyrrole and arylglyoxylic acids in the presence of K2S2O8at 90 C is reported affording dipyrromethanes in very good yields. Unlike an excess pyrrole traditionally used in dipyrromethane synthesis, the current method uses a stoichiometric amount of pyrrole avoiding any use of Br?nsted or Lewis acid. A gram scale synthesis of 5-phenyldipyrromethane is also achieved demonstrating potential scale up of dipyrromethanes using this method feasible. Subsequently, dipyrromethanes were converted to A4tetraarylporphyrins also in the presence of K2S2O8at 90C. A direct synthesis of A4-tetraphenylporphyrin from excess pyrrole and phenylglyoxylic acid in the presence of K2S2O8 at 90C is also reported.

Synthesis of 5,15-diarylporphyrins via orthoesters condensation with aryldipyrromethanes

Abada, Zahra,Ferrié, Laurent,Akagah, Bernardin,Lormier, Anh Tuan,Figadre, Bruno

scheme or table, p. 3175 - 3178 (2011/06/28)

General access to 5,15-diarylporphyrins in two steps is described. Generalization of this approach to tetra-substituted porphyrins allows the reproducible preparation of compounds, in some cases with high yields for porphyrins, which can be used in photodynamic therapy (PDT) in cancer today.

Synthetic porphyrins bearing β-propionate chains as photosensitizers for photodynamic therapy

Pereira, Nelson,Serra, Arménio C.,Pineiro, Marta,Gonsalves, António M. D'A. Rocha,Abrantes, Margarida,Laranjo, Mafalda,Botelho, Filomena

experimental part, p. 438 - 445 (2010/12/18)

Porphyrins with different numbers of β-propionate chains mimicking natural porphyrins were prepared via the 2+2 MacDonald type approach. Photodynamic activity against WiDr colon adenocarcinoma cells showed that activity is related to the number of β-propi

Fast and eco-friendly synthesis of dipyrromethanes by H2SO4 SiO2 catalysis under solvent-free conditions

Zhang, Yan,Liang, Jun,Shang, Zhicai

experimental part, p. 259 - 262 (2010/10/21)

For the first time, sillica-supported sulfuric acid has been used as a heterogeneous, reusable and efficient catalystat room temperature to give the corresponding dipyrromethanes in a very short reaction time. The new reactionprocedure is simple and solvent is not required.

Improved synthesis of meso substituted 21-Oxa and 2l-Thia tetra phenyl porphyrins

Srinivasan, Alagar,Sridevi, Bashyam,Reddy, Mereddy Venkat Ram,Narayanan, Seenichamy Jeyaprakash,Chandrashekar, Tavarekere K.

, p. 4149 - 4152 (2007/10/03)

An efficient method for the exclusive formation of 21-Oxa and 21-Thia tetra phenyl porphyrins in high yields by condensation of dipyrromethane and furan or thiophene diols is described.

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