3311-49-7 Usage
Structure
Cyclic amine with a seven-membered ring
Explanation
The compound has a closed loop or ring structure, with nitrogen (N) as part of the ring. The ring consists of seven atoms, making it a seven-membered ring.
Explanation
A chemical compound is a substance formed when two or more chemical elements are chemically bonded together in a fixed proportion.
Explanation
The compound is used as a building block to create various other compounds in the pharmaceutical and organic synthesis industries.
Explanation
It serves as an intermediate, a substance that is produced or consumed during a chemical reaction, in the production of pesticides and other industrial chemicals.
Explanation
Due to its unique structure and reactivity, the compound has potential applications in the field of medicine and drug development.
Explanation
As a highly versatile compound, 1H-Azepine, hexahydro-2,2-dipropylhas a broad spectrum of potential uses across various industries.
Explanation
The compound's unique structure contributes to its high reactivity, making it suitable for use in various chemical reactions and applications.
Type
Chemical compound
Application
Pharmaceutical and organic synthesis
Intermediate
Production of pesticides and industrial chemicals
Potential applications
Medicine and drug development
Versatility
Wide range of potential uses
Reactivity
Highly reactive
Check Digit Verification of cas no
The CAS Registry Mumber 3311-49-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,1 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3311-49:
(6*3)+(5*3)+(4*1)+(3*1)+(2*4)+(1*9)=57
57 % 10 = 7
So 3311-49-7 is a valid CAS Registry Number.
3311-49-7Relevant academic research and scientific papers
Reaction of Organolithium Reagents with Lactim Ethers: Preparation of Cyclic 2-Alkyl Imines or 2,2-Dialkyl Amines
Zezza, Charles A.,Smith, Michael B.,Ross, Betsy A.,Arhin, Akwasi,Cronin, Patricia L. E.
, p. 4397 - 4399 (2007/10/02)
The reaction of lactim ethers 1-3 with organolithium reagents has been found to be an effective method for the preparation of cyclic 2-alkyl imines 4-6.The method is most effective for the preparation of 2-aryl and sterically hindered 2-alkyl imines.In addition, treatment of 1-3 with excess organolithium provides a facile route to the rare cyclic 2,2-dialkyl amine derivatives 7-9.These reactions are characterized by mild reaction conditions and good yields and constitute a superior route to the title compounds.
