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3-[1-(4-methoxyphenyl)-2-nitropropyl]-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95021-29-7

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95021-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95021-29-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,0,2 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 95021-29:
(7*9)+(6*5)+(5*0)+(4*2)+(3*1)+(2*2)+(1*9)=117
117 % 10 = 7
So 95021-29-7 is a valid CAS Registry Number.

95021-29-7Downstream Products

95021-29-7Relevant academic research and scientific papers

Thermal and microwave-assisted conjugate additions of indole on electron-deficient nitro-olefins

Kusurkar, Radhika S.,Alkobati, Nabil A. H.,Gokule, Anita S.,Chaudhari, Purnima M.,Waghchaure, Prasad B.

, p. 1075 - 1081 (2006)

Conjugate addition of indole on nitro-olefins was carried out by three different methods: (i) thermal heating in a sealed tube, (ii) reaction with indolyl magnesium iodide, and (iii) microwave irradiation. Comparison of the results indicated that the micr

One-Pot Synthesis of 3-(2-Fluoroalkenyl)indoles

Aldoshin, Alexander S.,Tabolin, Andrey A.,Ioffe, Sema L.,Nenajdenko, Valentine G.

, p. 4384 - 4396 (2019/07/03)

An unprecedented one-pot synthesis of 3-(fluoroalkenyl)indoles was developed. This process involves a catalyst-free Michael addition of β-fluoro-β-nitrostyrenes to indoles in neat followed by elimination of HNO2 using DBU as a base. The effectiveness of this approach was demonstrated through the preparation of variety of target products in up to 75 % isolated yield.

Use of the Pictet-Spengler reaction for the synthesis of 1,4-disubstituted-1,2,3,4-tetrahydro-β-carbolines and 1,4-disubstituted-β-carbolines: formation of γ-carbolines

Kusurkar, Radhika S.,Alkobati, Nabil A.H.,Gokule, Anita S.,Puranik, Vedavati G.

, p. 1654 - 1662 (2008/09/17)

Microwave-assisted conjugate addition of indole on nitro-olefins furnished nitro compounds, which were reduced to tryptamines. Further, by using Pictet-Spengler condensation, new 1,4-disubstituted-1,2,3,4-tetrahydro-β-carbolines were synthesized in diaste

Conjugate addition of indoles to nitroalkenes promoted by basic alumina in solventless conditions

Ballini, Roberto,Clemente, Roberto Rabanedo,Palmieri, Alessandro,Petrini, Marino

, p. 191 - 196 (2007/10/03)

Basic alumina is found to promote the conjugate addition of indoles to nitroalkenes in solventless conditions at 60°C. Nitroalkenes can be replaced by nitro alcohols that are converted into nitroolefins under the reaction conditions. Alternatively, a tand

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