161862-09-5 Usage
Description
3-Amino-1-piperidin-1-yl-propan-1-one is a chemical compound that belongs to the class of organic compounds known as piperidines. These compounds are characterized by a piperidine ring, which is a saturated aliphatic six-member ring with one nitrogen atom and five carbon atoms. The chemical structure of 3-Amino-1-piperidin-1-yl-propan-1-one features functional groups such as an amino group and a ketone, contributing to its versatile reactivity and structural complexity.
Uses
Used in Pharmaceutical Industry:
3-Amino-1-piperidin-1-yl-propan-1-one is used as an intermediate compound for the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
3-Amino-1-piperidin-1-yl-propan-1-one is used as a building block in the creation of agrochemicals, such as pesticides and herbicides. Its chemical properties enable the design of effective compounds for agricultural use.
Used in Chemical Research:
3-Amino-1-piperidin-1-yl-propan-1-one serves as a valuable research tool in the field of organic chemistry. Its reactivity and structural features make it an interesting subject for studying chemical reactions and mechanisms.
It is important to handle 3-Amino-1-piperidin-1-yl-propan-1-one with care, following safety guidelines, as its health effects are largely unknown. This precaution is necessary to ensure the safety of those working with this compound in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 161862-09-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,8,6 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 161862-09:
(8*1)+(7*6)+(6*1)+(5*8)+(4*6)+(3*2)+(2*0)+(1*9)=135
135 % 10 = 5
So 161862-09-5 is a valid CAS Registry Number.
InChI:InChI=1S/C8H16N2O/c9-5-4-8(11)10-6-2-1-3-7-10/h1-7,9H2
161862-09-5Relevant articles and documents
Methylene C(sp3)-H β,β′-Diarylation of Cyclohexanecarbaldehydes Promoted by a Transient Directing Group and Pyridone Ligand
Bull, James A.,St John-Campbell, Sahra,White, Andrew J. P.
, (2020/03/10)
A hindered β-amino amide transient directing group effects di-trans-arylation of cyclohexanecarbaldehydes. The amide N-substituents are shown to affect yield and can enhance the rate of arylation compared with the α-amino acid. Addition of a pyridone ligand further enhanced reactivity. The reaction is successful for a range of aryl iodides, and various substituted cyclohexane carboxaldehydes, providing functionalized products from simple feedstocks. A mechanism is proposed evoking a transient enamine.
