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2-[(1H-indol-3-yl)(pyridin-2-yl)methyl]-3-hydroxy-5,5-dimethylcyclohex-2-enone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

537010-97-2

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537010-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 537010-97-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,7,0,1 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 537010-97:
(8*5)+(7*3)+(6*7)+(5*0)+(4*1)+(3*0)+(2*9)+(1*7)=132
132 % 10 = 2
So 537010-97-2 is a valid CAS Registry Number.

537010-97-2Downstream Products

537010-97-2Relevant academic research and scientific papers

Palladium oxide-decorated mesoporous silica on graphene oxide nanosheets as a heterogeneous catalyst for the synthesis of β-substituted indole derivatives

Sah, Digvijay,Shabir, Javaid,Surabhi,Gupta, Padmini,Mozumdar, Subho

, p. 5644 - 5658 (2021)

In this work, an efficient and facile strategy has been adopted for the stepwise synthesis of the RGO-MSiO2/PdO hybrid nanomaterial (HY-NM). Herein, a hybrid nanostructure of mesoporous silica over graphene oxide (GO) sheets has been developed

Heterogenization of amine-functionalized ionic liquids using graphene oxide as a support material: A highly efficient catalyst for the synthesis of 3-substituted indoles: Via Yonemitsu-type reaction

Garkoti, Charu,Shabir, Javaid,Gupta, Padmini,Sharma, Manisha,Mozumdar, Subho

, p. 15545 - 15554 (2017/12/15)

In the present study, heterogenization of amine-functionalized ionic liquids was developed via covalent immobilization of 2-chloroethylamine on imidazole modified graphene oxide (GO) sheets. The prepared material was characterized by various physicochemical techniques such as Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffraction (XRD), thermogravimetric analysis (TGA), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and energy-dispersive X-ray (EDX) spectroscopy. The prepared material was employed as an efficient heterogeneous catalyst for the synthesis of 3-substituted indoles via Yonemitsu-type reaction. The catalyst could be easily separated from the reaction mixture through centrifugation and could be reused for seven consecutive cycles without any appreciable loss in its catalytic activity.

Three-component reactions of aromatic aldehydes and two different nucleophiles and their leaving ability-determined downstream conversions of the products

Li, Minghao,Taheri, Amir,Liu, Meng,Sun, Shaohuan,Gu, Yanlong

, p. 537 - 556 (2014/05/20)

Many three-component reactions of aromatic aldehydes with activated methylene derivatives and an associated nucleophile have been developed by using l-proline as the catalyst. Nucleophiles, such as indoles, thiophenols, mercaptans, 2-methylfuran and benze

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