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1H-Pyrrole-2-acetonitrile, 1-methyl-5-(4-nitrobenzoyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26171-27-7

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26171-27-7 Usage

Molecular Structure

1H-Pyrrole-2-acetonitrile, 1-methyl-5-(4-nitrobenzoyl)is a chemical compound that consists of a pyrrole ring and an acetonitrile group substituted with a 1-methyl-5-(4-nitrobenzoyl) moiety.

Usage

1H-Pyrrole-2-acetonitrile, 1-methyl-5-(4-nitrobenzoyl)- is commonly used in organic synthesis and pharmaceutical research as a building block for the synthesis of various biologically active compounds.

Potential Applications

1H-Pyrrole-2-acetonitrile, 1-methyl-5-(4-nitrobenzoyl)has potential application in the development of pharmaceuticals and agrochemicals.

Reactivity

1H-Pyrrole-2-acetonitrile, 1-methyl-5-(4-nitrobenzoyl)- has diverse reactivity and functional groups, which makes it useful in the synthesis of various biologically active compounds.

Safety

It is important to handle 1H-Pyrrole-2-acetonitrile, 1-methyl-5-(4-nitrobenzoyl)- with care and follow proper safety protocols due to its potential toxicity and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 26171-27-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,7 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 26171-27:
(7*2)+(6*6)+(5*1)+(4*7)+(3*1)+(2*2)+(1*7)=97
97 % 10 = 7
So 26171-27-7 is a valid CAS Registry Number.

26171-27-7Relevant academic research and scientific papers

1,3,6-trihydro-6-aza-3-oxapentalen-2-one derivatives for the treatment of neoplasia

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, (2008/06/13)

1,3,6-Trihydro-6-Aza-3-Oxapentalen-2-One Derivatives for inhibiting neoplastic conditions.

Preparation of 5-(arylcyanohydroxymethyl)-1-loweralkylpyrrole-2-acetic acid derivatives

-

, (2008/06/13)

5-(Arylcyanohydroxymethyl)-1-loweralkylpyrrole-2-acetic acid derivatives are prepared by the protic acid catalyzed reaction of aroylcyanides with 1-loweralkylpyrrole-2-acetic acid derivatives, which is then converted by treatment with alkali metal hydroxides or heat to form 5-aroyl-1-loweralkylpyrrole-2-acetic acid or derivatives thereof.

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