26956-47-8 Usage
General Description
1-Benzyl-4-hydroxy-5-azaindole is a chemical compound with a molecular formula C14H12N2O. It is a heterocyclic organic compound that contains a five-membered ring with nitrogen and oxygen atoms. 1-BENZYL-4-HYDROXY-5-AZAINDOLE has potential applications in pharmaceutical and medicinal chemistry due to its ability to interact with biological systems and potentially exhibit therapeutic properties. Its aromatic benzyl group and hydroxy substituent contribute to its chemical and biological properties, making it a subject of interest in drug discovery and development. Additionally, its unique structural features make it a valuable building block for the synthesis of more complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 26956-47-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,5 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 26956-47:
(7*2)+(6*6)+(5*9)+(4*5)+(3*6)+(2*4)+(1*7)=148
148 % 10 = 8
So 26956-47-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H12N2O/c17-14-12-7-9-16(13(12)6-8-15-14)10-11-4-2-1-3-5-11/h1-9H,10H2,(H,15,17)
26956-47-8Relevant articles and documents
One-pot synthesis of fused 2-pyridones from heteroarylacrylic acid via curtius rearrangement & microwave-assisted thermal electrocyclization
Nishiyama, Takashi,Hatae, Noriyuki,Hayashi, Kaori,Obata, Manami,Taninaka, Kimiko,Yamane, Masahiro,Oda, Shota,Abe, Takumi,Ishikura, Minoru,Hibino, Satoshi,Choshi, Tominari
, p. 251 - 267 (2017/07/28)
We investigated the one-pot synthesis of several fused 2-pyridone ring systems based on a Curtius rearrangement, followed by a microwave-assisted thermal electrocyclization of a 2-aza-6?-electron system including isocyanate. We synthesized seven heterocyclic compounds containing a fused 2-pyridone ring. In these results, the one-pot synthesis of fused 2-pyridone ring system 5 from (E)-acrylic acids 1 under microwave irradiation conditions was more effective than the conventional reaction conditions in terms of the yield and the reaction time.