73051-88-4

Usage

Uses

Used in Pharmaceutical Industry:
PMM is used as a building block in the synthesis of various pharmaceutical compounds. Its versatile chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
PMM is also used as a building block in the synthesis of agrochemical compounds, contributing to the development of new pesticides and other agricultural products.
Used in Asymmetric Synthesis:
PMM has been studied for its potential as a chiral auxiliary in asymmetric synthesis, which is an important technique in the production of enantiomerically pure compounds. This application can lead to the development of more efficient and selective synthetic methods.
Used in Pharmacology:
PMM has been investigated for its pharmacological activities, including its potential as an analgesic and anti-inflammatory agent. This research could lead to the development of new medications for the treatment of pain and inflammation.
Overall, PMM is a valuable chemical compound with wide-ranging potential in various industries, including pharmaceuticals, agrochemicals, asymmetric synthesis, and pharmacology. Its diverse applications make it an important compound for ongoing research and development.

InChI:InChI=1/C11H15NO/c13-9-10-5-1-2-6-11(10)12-7-3-4-8-12/h1-2,5-6,13H,3-4,7-9H2

Upstream product

• 58028-74-3 2-pyrrolidin-1-ylbenzaldehyde 

Downstream Products

• 87067-06-9 1,2,3,3a-tetrahydro-5H-pyrrolo<1,2-a><3,1>benzoxazine 
• 110405-82-8 1-[2-(chloromethyl)phenyl]piperidine hydrochloride 
• 58028-74-3 2-pyrrolidin-1-ylbenzaldehyde 

Relevant academic research and scientific papers

Divergent α-functionalization of cyclic amines: Via ring construction by molecular O2oxidized dearomatization and ring deconstruction by aromatization-driven C-C σ-bond cleavage

An efficient approach to achieve the divergent α-C(sp3)-H functionalization of cyclic amines through a rationally designed ring construction and ring deconstruction strategy was developed. A variety of spiro cyclohexadienone decorated cyclic amines were o

Study on the scope of tert-amino effect: New extensions of type 2 reactions to bridged biaryls

Thermal isomerization of aminomethyl- or oxygen-bridged biphenyl systems possessing dicyanovinyl and sec-amino groups in ortho- and ortho0-positions was investigated. Both systems underwent cyclization via tert-amino effect. Thus, 2-(2-{[2-(sec-amino)benz

An efficient microwave-assisted solvent-free synthesis of pyrido-fused ring systems applying the tert-amino effect

Significant improvements in the synthesis of pyrido-fused heterocycles were observed when performing the reaction under solvent-free conditions, applying the tert-amino effect as the key ring closure methodology. An unexpected cyclization of ortho-(1′-aza

Neighbourgroup Participation with the Dehydrogenation of Cyclic Amines of the o-Substituted Aniline Type

The 2-Aminobenzylalcohols 1a - c produced with mercury-edta dehydrogenation the lactams 6a - c; the pipecoline 2b yielded the benzoxazine 3b indicating the participation of the nucleophilic hydroxymethyl group. The 2-aminobenzaldehydes showed a different behaviour in dependence on the ring size of the amine part: 7a, b led - via intermediate reaction of the hemiaminal 9 with the electrophilic formyl function - to the lactams 11a, b, while 7c gave rise to the aminoaldehyde 12 as major product and similarly the pipecoline 15 to the aminoketone 16. From 2′-(4-morpholinyl)-acetophenone (22) were received the lactam 31 and the aminoethanol 32, both by a twofold dehydrogenation.