6361-33-7 Usage
Description
N-(1-Naphtyl)benzenemethaneamine, also known as N-(1-naphthyl)benzylamine, is a chemical compound with the molecular formula C18H17N. It is a derivative of benzene and naphthalene, characterized by its yellowish solid appearance at room temperature and solubility in organic solvents such as ethanol and diethyl ether. N-(1-Naphtyl)benzenemethaneamine is widely utilized in organic synthesis and serves as a chemical intermediate in the production of pharmaceuticals and dyes. Its potential as a reagent in the study and analysis of various organic compounds, along with its anti-inflammatory and analgesic properties, makes it a promising candidate for the development of new therapeutic agents.
Uses
Used in Organic Synthesis:
N-(1-Naphtyl)benzenemethaneamine is used as a chemical intermediate for the synthesis of various organic compounds, contributing to the development of new pharmaceuticals and dyes.
Used in Pharmaceutical Production:
In the pharmaceutical industry, N-(1-Naphtyl)benzenemethaneamine is utilized as a key component in the manufacturing process of certain drugs, leveraging its chemical properties to enhance the efficacy and function of these medications.
Used in Dye Production:
N-(1-Naphtyl)benzenemethaneamine is also employed in the production of dyes, where its chemical structure contributes to the color and stability of the final product.
Used in Research and Analysis:
N-(1-Naphtyl)benzenemethaneamine is used as a reagent in the study and analysis of various organic compounds, aiding researchers in understanding the properties and reactions of different chemical entities.
Used in Therapeutic Agent Development:
Due to its anti-inflammatory and analgesic properties, N-(1-Naphtyl)benzenemethaneamine is of interest in the development of new therapeutic agents, potentially offering novel treatments for conditions that involve inflammation and pain.
Check Digit Verification of cas no
The CAS Registry Mumber 6361-33-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,6 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6361-33:
(6*6)+(5*3)+(4*6)+(3*1)+(2*3)+(1*3)=87
87 % 10 = 7
So 6361-33-7 is a valid CAS Registry Number.
6361-33-7Relevant articles and documents
Hydride transfer reactivity of tetrakis(trimethylphosphine)(hydrido) (nitrosyl)molybdenum(0)
Zhao, Yin,Schmalle, Helmut W.,Fox, Thomas,Blacque, Olivier,Berke, Heinz
, p. 73 - 85 (2006)
The tetrakis(trimethylphosphine) molybdenum nitrosyl hydrido complex trans-Mo(PMe3)4(H)(NO) (2) and the related deuteride complex trans-Mo(PMe3)4(D)(NO) (2a) were prepared from trans-Mo(PMe3)4/s
Iron-catalyzed N-alkylation of aromatic amines via borrowing hydrogen strategy
Chen, Hui,Wang, Qingfu,Liu, Tingting,Chen, Haitao,Zhou, Duo,Qu, Fengbo
, p. 877 - 884 (2021/02/16)
Earth-abundant transition metals could be used as a noble metal replacement in catalysis not only for different catalytic reactivity but environmentally benign methodology. We report here on the iron-catalyzed synthesis of N-alkylated amines via borrowing hydrogen strategy and differently functionalized aniline derivatives are alkylated in good yields.
[(PPh3)2NiCl2]-Catalyzed C-N bond formation reaction via borrowing hydrogen strategy: Access to diverse secondary amines and quinolines
Donthireddy,Pandey, Vipin K.,Rit, Arnab
, p. 6994 - 7001 (2021/06/09)
Commercially available [(PPh3)2NiCl2] was found to be an efficient catalyst for the mono-N-alkylation of (hetero)- A romatic amines, employing alcohols to deliver diverse secondary amines, including the drug intermediates chloropyramine (5b) and mepyramine (5c), in excellent yields (up to 97%) via the borrowing hydrogen strategy. This method shows a superior activity (TON up to 10000) with a broad substrate scope at a low catalyst loading of 1 mol % and a short reaction time. Further, this strategy is also successful in accessing various quinoline derivatives following the acceptorless dehydrogenation pathway.