6281-00-1 Usage
Description
N-butylnaphthalen-1-amine is a chemical compound with the molecular formula C14H15N, classified as an amine derived from naphthalene, a polycyclic aromatic hydrocarbon. The "N-butylnaphthalen-1" part of the name signifies that the amine is attached to the naphthalene ring at the 1 position, while "butyl" denotes the four-carbon alkyl group attached to the nitrogen atom. N-butylnaphthalen-1-amine is frequently utilized as a building block in the synthesis of other organic compounds and may also serve as a laboratory reagent or intermediate in chemical reactions. However, due to potential health risks, it is crucial to handle this chemical with care and adhere to proper safety precautions and handling procedures.
Uses
Used in Organic Synthesis:
N-butylnaphthalen-1-amine is used as a building block for the synthesis of other organic compounds, contributing to the creation of a variety of chemical products due to its unique structure and reactivity.
Used in Laboratory Research:
As a laboratory reagent, N-butylnaphthalen-1-amine is employed in various chemical experiments and analyses, facilitating the study of chemical reactions and the development of new methodologies in organic chemistry.
Used in Chemical Reactions as an Intermediate:
N-butylnaphthalen-1-amine serves as an intermediate in chemical reactions, playing a crucial role in the synthesis pathways of complex organic molecules, which may have applications in pharmaceuticals, materials science, or other specialized industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6281-00-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6281-00:
(6*6)+(5*2)+(4*8)+(3*1)+(2*0)+(1*0)=81
81 % 10 = 1
So 6281-00-1 is a valid CAS Registry Number.
6281-00-1Relevant articles and documents
A one-pot azido reductive tandem mono-N-alkylation employing dialkylboron triflates: Online ESI-MS mechanistic investigation
Shankaraiah, Nagula,Markandeya, Nagula,Srinivasulu, Vunnam,Sreekanth, Kokkonda,Reddy, Ch. Sanjeeva,Santos, Leonardo S.,Kamal, Ahmed
experimental part, p. 7017 - 7026 (2011/10/10)
An efficient one-pot reductive tandem mono-N-alkylation of both aromatic and aliphatic azides using dialkylboron triflates as alkylating agents has been examined under standardized reaction conditions. This methodology after optimization has been employed toward the syntheses of various secondary alkyl as well as aryl amines, including the synthesis of N10-butylated pyrrolo[2,1-c][1,4]benzodiazepine-5,11-diones via in situ azido reductive-cyclization process. This protocol is particularly attractive to provide an environmentally benign and practical method for mono-N-alkylation from organic azides without the use of toxic catalysts or corrosive alkylating agents. In addition, the mechanistic aspects have been investigated and the intermediates associated with this selective transformation have been intercepted and characterized by online monitoring of the reaction by ESI-MS/MS.
