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1H-Pyrrolo[2,3-b]pyridine-1-acetonitrile is a heterocyclic compound characterized by a pyrrolo[2,3-b]pyridine core, which is a fused ring system consisting of a pyrrole and a pyridine. The molecule features a nitrile group (-CN) attached to the acetonitrile moiety, which is a derivative of acetone where one hydrogen atom is replaced by a nitrile group. This chemical structure is of interest in medicinal chemistry and drug design due to its potential to form stable complexes with various biological targets. The compound's unique electronic properties and structural features make it a candidate for further exploration in the development of new pharmaceuticals, particularly those targeting the central nervous system or other biological processes where such heterocyclic systems are known to be active.

4414-72-6

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4414-72-6 Usage

Heterocyclic compound

Pyrrole and pyridine rings The compound contains two heterocyclic rings, a pyrrole ring and a pyridine ring, which contribute to its chemical properties and potential pharmacological activities.

Pyrrole ring fused to a pyridine ring

Structural feature The pyrrole ring is fused to the pyridine ring, creating a unique structure that influences the compound's properties and potential applications.

Acetonitrile group

Functional group The presence of an acetonitrile group (CN) in the compound adds to its reactivity and potential for use in the synthesis of bioactive molecules.

Pharmaceutical industry use

Building block for synthesis 1H-Pyrrolo[2,3-b]pyridine-1-acetonitrile is commonly used as a building block in the pharmaceutical industry for the synthesis of various bioactive molecules.

Potential biological activities

Inhibitor of protein kinases The compound has been reported to have potential biological activities, including the ability to inhibit protein kinases, which are involved in various cellular processes.

Potential anti-cancer agent

Therapeutic application 1H-Pyrrolo[2,3-b]pyridine-1-acetonitrile has shown potential as an anti-cancer agent, making it a valuable compound in medicinal chemistry research.

Unique structure and pharmacological properties

Importance in research The compound's unique structure and potential pharmacological properties make it an important and valuable compound in medicinal chemistry research.

Check Digit Verification of cas no

The CAS Registry Mumber 4414-72-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,1 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4414-72:
(6*4)+(5*4)+(4*1)+(3*4)+(2*7)+(1*2)=76
76 % 10 = 6
So 4414-72-6 is a valid CAS Registry Number.

4414-72-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-pyrrolo[2,3-b]pyridin-1-ylacetonitrile

1.2 Other means of identification

Product number -
Other names 1h-pyrrolo[2,3-b]pyridine-1-acetonitrile

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4414-72-6 SDS

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