41717-32-2 Usage
Description
2-CyanoBenzofuran, also known as 1-Benzofuran-2-carbonitrile, is an organic compound with the molecular formula C8H5NO. It is a heterocyclic compound that consists of a benzene ring fused to a furan ring, with a nitrile group (C≡N) attached to the second position. 2-CYANOBENZOFURAN is a valuable intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity.
Uses
Used in Pharmaceutical Industry:
2-CyanoBenzofuran is used as a key intermediate in the synthesis of imidazoline I1 and I2 selective ligands for the imidazoline and α-adrenergic receptors. These ligands play a crucial role in the development of drugs targeting these receptors, which are involved in various physiological processes, including blood pressure regulation, pain modulation, and neuroprotection.
Used in Antiparasitic and Antifungal Agents:
2-CyanoBenzofuran is also utilized in the synthesis of antiparasitic and antifungal arylthiazolines. These compounds exhibit potent activity against a wide range of parasites and fungi, making them valuable in the development of treatments for parasitic and fungal infections.
Check Digit Verification of cas no
The CAS Registry Mumber 41717-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,7,1 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 41717-32:
(7*4)+(6*1)+(5*7)+(4*1)+(3*7)+(2*3)+(1*2)=102
102 % 10 = 2
So 41717-32-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H5NO/c10-6-8-5-7-3-1-2-4-9(7)11-8/h1-5H
41717-32-2Relevant articles and documents
Iridium-catalyzed hydrogen transfer: Synthesis of substituted benzofurans, benzothiophenes, and indoles from benzyl alcohols
Anxionnat, Bruno,Gomez Pardo, Domingo,Ricci, Gino,Rossen, Kai,Cossy, Janine
supporting information, p. 3876 - 3879 (2013/09/02)
An iridium-catalyzed hydrogen transfer has been developed in the presence of p-benzoquinone, allowing the synthesis of a diversity of substituted benzofurans, benzothiophenes, and indoles from substituted benzylic alcohols.
