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3-(2-oxo-2-phenylethyl)isobenzofuran-1(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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72897-60-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72897-60-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,9 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 72897-60:
(7*7)+(6*2)+(5*8)+(4*9)+(3*7)+(2*6)+(1*0)=170
170 % 10 = 0
So 72897-60-0 is a valid CAS Registry Number.

72897-60-0Downstream Products

72897-60-0Relevant academic research and scientific papers

The antileishmanial potential of C-3 functionalized isobenzofuranones against Leishmania (Leishmania) Infantum Chagasi

Pereira, Wagner Luiz,De Souza Vasconcellos, Raphael,Mariotini-Moura, Christiane,Gomes, Rodrigo Saar,De Cássia Firmino, Rafaela,Da Silva, Adalberto Manoel,Júnior, Abelardo Silva,Bressan, Gustavo Costa,Almeida, Márcia Rogéria,Afonso, Luís Carlos Crocco,Teixeira, Róbson Ricardo,Fietto, Juliana Lopes Rangel,McPhee, Derek J.

, p. 22435 - 22444 (2016/01/25)

Leishmaniases are diseases caused by protozoan parasites of the genus Leishmania. Clinically, leishmaniases range from cutaneous to visceral forms, with estimated global incidences of 1.2 and 0.4 million cases per year, respectively. The treatment of thes

An approach to dihydroisoindolobenzodiazepinones - Three-dimensional molecular frameworks

Yaremenko, Anatoliy G.,Shelyakin, Vyacheslav V.,Volochnyuk, Dmitriy M.,Rusanov, Eduard B.,Grygorenko, Oleksandr O.

, p. 1195 - 1197 (2013/03/13)

A concise two-step procedure is developed for the preparation of dihydroisoindolobenzodiazepinones, which represent derivatives of three-dimensional molecular frameworks derived from classical privileged structures of medicinal chemistry. The method commences from the readily available starting materials (i.e., 2-formylbenzoic acid, o-phenylenediamine, and various ketones) and enables the synthesis of the title compounds in 58-82% overall yields.

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