292151-99-6 Usage
Description
(2'-METHOXY[1,1'-BIPHENYL]-2-YL)METHANAMINE is a chemical compound belonging to the amine family, characterized by its molecular formula C14H15NO. It features a biphenyl group with a methoxy group attached to the 2' position of one of the benzene rings, making it a versatile building block in the synthesis of pharmaceutical drugs and other organic compounds.
Uses
Used in Pharmaceutical Research:
(2'-METHOXY[1,1'-BIPHENYL]-2-YL)METHANAMINE is used as a key building block in the synthesis of various pharmaceutical drugs and other organic compounds. Its potential biological activity makes it a valuable tool in drug discovery and development.
Used in Drug Synthesis:
In the pharmaceutical industry, (2'-METHOXY[1,1'-BIPHENYL]-2-YL)METHANAMINE is used as a precursor for the development of new drugs, contributing to the advancement of medicinal chemistry and the creation of innovative therapeutic agents.
Safety and Handling:
It is crucial to handle and store (2'-METHOXY[1,1'-BIPHENYL]-2-YL)METHANAMINE in accordance with proper safety and handling procedures to minimize potential health hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 292151-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,2,1,5 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 292151-99:
(8*2)+(7*9)+(6*2)+(5*1)+(4*5)+(3*1)+(2*9)+(1*9)=146
146 % 10 = 6
So 292151-99-6 is a valid CAS Registry Number.
292151-99-6Relevant articles and documents
Synthesis of highly substituted fluorenones via metal-free TBHP-promoted oxidative cyclization of 2-(aminomethyl)biphenyls. Application to the total synthesis of nobilone
Bracher, Franz,Jourjine, Ilya A. P.,Krau?, Jürgen,Zeisel, Lukas
, p. 2668 - 2679 (2021/11/30)
Highly substituted fluorenones are readily prepared in mostly fair to good yields via metal- and additive-free TBHP-promoted cross-dehydrogenative coupling (CDC) of readily accessible N-methyl-2-(aminomethyl)biphenyls and 2-(aminomethyl)biphenyls. This methodology is compatible with numerous functional groups (methoxy, cyano, nitro, chloro, and SEM and TBS-protective groups for phenols) and was further utilized in the first total synthesis of the natural product nobilone.
