1336918-65-0 Usage
Chemical structure
The compound contains a naphthalene ring and a boron-containing diazaborinine ring.
Type of compound
Heterocyclic compound.
Potential applications
Organic synthesis, materials science, and as a catalyst.
Aromatic ring system
The compound has an aromatic ring system, which makes it valuable for the synthesis of new organic compounds.
Potential for functionalization
The compound can be further modified, which makes it a valuable building block for the synthesis of new organic compounds.
Unique structure
The compound has a unique structure that makes it a promising target for further research and development in the field of organic and materials chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1336918-65-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,6,9,1 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1336918-65:
(9*1)+(8*3)+(7*3)+(6*6)+(5*9)+(4*1)+(3*8)+(2*6)+(1*5)=180
180 % 10 = 0
So 1336918-65-0 is a valid CAS Registry Number.
1336918-65-0Relevant articles and documents
Catalyst-free and eco-friendly synthesis of masked haloarylboronic acids R (alkyl or aryl)-B(dan) on water
Liao, Siwei,Hu, Xueyuan,Li, Yanwu,Wang, Xuetong,Li, Dan,Wang, Qiang,Wang, Yin,Huang, Xin,Xu, Ping,Wu, Huili,Li, Xianliang,Yuan, Jianyong
supporting information, (2021/05/31)
An environment-friendly methodology for the synthesis of R (alkyl or aryl)-B(dan) on water is described. 1,8-diamino naphthalene(danH2) was reacted with different types of organoboronic acids to furnish the products in moderate to excellent yields. A multi-gram scale reaction is also performed to ensure the scalability of the reaction.
Iron catalysis and water: A synergy for refunctionalization of boron
Wood, John L.,Marciasini, Ludovic D.,Vaultier, Michel,Pucheault, Mathieu
, p. 551 - 555 (2014/03/21)
A new catalytic system has been optimized to promote the conversion of boron species into others. FeCl3 associated with imidazole and water favors boron refunctionalization under mild conditions. Georg Thieme Verlag Stuttgart New York.
