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4-bromo-2-(di(1H-indol-3-yl)methyl) phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

893250-54-9

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893250-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 893250-54-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,3,2,5 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 893250-54:
(8*8)+(7*9)+(6*3)+(5*2)+(4*5)+(3*0)+(2*5)+(1*4)=189
189 % 10 = 9
So 893250-54-9 is a valid CAS Registry Number.

893250-54-9Downstream Products

893250-54-9Relevant academic research and scientific papers

Water-mediated green and efficient synthesis of bis(Indolyl)methanes using ammonium iron(II) sulfate

Kadu, Vikas D.,Nadimetla, Dinesh N.,Hublikar, Mahesh G.,Raut, Dattatraya G.,Bhosale, Raghunath B.

, p. 61 - 67 (2020)

An efficient protocol for the synthesis of symmetrical 3,3’-bis(indolyl)arylmethanes catalyzed by green and easily available ammonium iron(II) sulfate (Mohr’s salt) has been developed in “green” water solvent afforded in excellent yield.

Green and efficient synthesis of aryl/alkylbis(indolyl)methanes using Expanded Perlite-PPA as a heterogeneous solid acid catalyst in aqueous media

Esmaielpour, Marzieh,Akhlaghinia, Batool,Jahanshahi, Roya

, p. 313 - 328 (2017/03/23)

Expanded Perlite-Polyphosphoric acid (EP-PPA) as a novel, efficient, recyclable and eco-benign heterogeneous catalyst has been applied for the green and rapid synthesis of aryl/alkylbis(indolyl)methanes, in water, in good to excellent yields. The catalyst

Biocatalysts for cascade reaction: Porcine pancreas lipase (PPL)-catalyzed synthesis of bis(indolyl)alkanes

Xiang, Ziwei,Liu, Zhiqiang,Chen, Xiang,Wu, Qi,Lin, Xianfu

, p. 937 - 945 (2013/10/22)

A cascade reaction between aldehydes and indole catalyzed by lipase from porcine pancreas Type II (PPL) in solvent mixture at 50 C was reported for the first time. Some control experiments had been designed to demonstrate that the PPL was responsible for

Micelle promoted synthesis of bis-(indolyl)methanes

Kumar, Krishnammagari S.,Reddy, Chinnapareddy B.,Krishna, Balam S.,Srinivasulu, Kambam,Reddy, Cirandur S.

experimental part, p. 294 - 299 (2012/08/08)

Abstract: Bis-(indolyl)methanes were synthesized by a simple, clean and highly efficient Tween-20 micelle promoted reaction of indole with aldehydes in water by the single step reaction. The absence of electrical double layer in the nonionic surfactant mi

Room-temperature synthesis of diindolylmethanes using silica-supported sulfuric acid as a reusable catalyst under solvent-free conditions

Zhang, Yan,Chen, Xiang,Liang, Jun,Shang, Zhi-Cai

experimental part, p. 2446 - 2454 (2011/08/07)

Efficient electrophilic substitution reactions of indoles with various aromatic and aliphatic aldehydes were carried out using a catalytic amount of H2SO4SiO2 under solvent-free conditions to afford the corresponding bis(indolyl)methanes in excellent yields.

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