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

1173111-08-4

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1173111-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1173111-08-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,1,1 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1173111-08:
(9*1)+(8*1)+(7*7)+(6*3)+(5*1)+(4*1)+(3*1)+(2*0)+(1*8)=104
104 % 10 = 4
So 1173111-08-4 is a valid CAS Registry Number.

1173111-08-4Downstream Products

1173111-08-4Relevant academic research and scientific papers

Turning on catalysis: Incorporation of a hydrogen-bond-donating squaramide moiety into a Zr metal-organic framework

McGuirk, C. Michael,Katz, Michael J.,Stern, Charlotte L.,Sarjeant, Amy A.,Hupp, Joseph T.,Farha, Omar K.,Mirkin, Chad A.

, p. 919 - 925 (2015)

Herein, we demonstrate that the incorporation of an acidic hydrogen-bond-donating squaramide moiety into a porous UiO-67 metal-organic framework (MOF) derivative leads to dramatic acceleration of the biorelevant Friedel-Crafts reaction between indole and

Synthesis of 3-(2-Nitroalkyl)pyrroles from sulfonylpyrroles and their conversion to 6-azaindole derivatives

Lancianesi, Stefano,Palmieri, Alessandro,Petrini, Marino

, p. 3285 - 3289 (2013/12/04)

The reaction of sulfonylpyrroles with nitroalkanes in the presence of KF/alumina generates 3-(2-nitroalkyl)pyrroles in good yields. These compounds can be converted into trisubstituted 6-azaindoles by a sequence of reactions comprising reduction of the ni

Simple and efficient Friedel-Crafts alkylation of 1H-indole with electron-deficient alkenes promoted by zinc acetate

Meshram, Harshadas Mitaram,Kumar, Dachepally Aravind,Reddy, Bandi Chennakesava

experimental part, p. 1002 - 1006 (2009/08/14)

An efficient method for the Friedel-Crafts alkylation of 1H-indole with nitro alkenes in the presence of zinc acetate is described. The procedure is applicable to a variety of nitro alkenes and substituted indoles, and the yields are very high.

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