183429-63-2

Basic information

• Product Name: METHYL 1-AMINO-1-CYCLOHEPTANECARBOXYLATE
• Synonyms: METHYL 1-AMINO-1-CYCLOHEPTANECARBOXYLATE;Methyl 1-amino-1-cycloheptanecarboxylate HCl;Methyl 1-aMinocycloheptanecarboxylate;Cycloheptanecarboxylic acid, 1-amino-, methyl ester
• CAS NO: 183429-63-2
• Molecular Formula: C9H17NO2
• Molecular Weight: 171.24
• Product Categories: pharmacetical
• Mol File: 183429-63-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 231.9 °C at 760 mmHg
• Flash Point: 98.6 °C
• Appearance: /
• Density: 1.02 g/cm³
• Storage Temp.: 2-8°C
• CAS DataBase Reference: METHYL 1-AMINO-1-CYCLOHEPTANECARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 1-AMINO-1-CYCLOHEPTANECARBOXYLATE(183429-63-2)
• EPA Substance Registry System: METHYL 1-AMINO-1-CYCLOHEPTANECARBOXYLATE(183429-63-2)

Safety Data

• Hazardous Substances Data: 183429-63-2(Hazardous Substances Data)

Usage

General Description

Methyl 1-amino-1-cycloheptanecarboxylate is an organic compound with the chemical formula C9H15NO2. It is a derivative of amino acid and is used in the pharmaceutical industry as a building block in the synthesis of various compounds, including drugs. METHYL 1-AMINO-1-CYCLOHEPTANECARBOXYLATE has a unique seven-membered cycloheptane ring structure and a methyl group attached to the amino group and a carboxylate group. It is synthesized through organic reactions and has various applications in medicinal chemistry, particularly in the development of new drugs and pharmaceuticals.

Upstream product

• 502-42-1 cycloheptanone 
• 67-56-1 methanol 
• 6949-77-5 1-aminocycloheptane-1-carboxylic acid 
• 123193-99-7 1-aminocycloheptanecarbonitrile 

Downstream Products

• 814254-62-1 (1-aminocycloheptyl)methanol 

Relevant articles and documents

Polycyclic Azetidines and Pyrrolidines via Palladium-Catalyzed Intramolecular Amination of Unactivated C(sp3)-H Bonds

A novel strategy to construct complex polycyclic nitrogen-containing heterocycles from aliphatic amines via picolinamide-assisted palladium-catalyzed C-H bond activation reaction was reported. The reaction exhibits broad substrate scope for the synthesis of various azabicyclic scaffolds, including azetidines and tropane-class alkaloids. Application of this method to naturally occurring (-)-cis-myrtanylamine, an unprecedented type of carbon-carbon bond activation, in which the electron-pair involved initiates an intramolecular "SN2-like" displacement of a cyclopalladium-fragment from a tertiary center, is described.

Anthranilimide-based glycogen phosphorylase inhibitors for the treatment of type 2 diabetes: 1. Identification of 1-amino-1-cycloalkyl carboxylic acid headgroups

Optimization of the amino acid residue within a series of anthranilimide-based glycogen phosphorylase inhibitors is described. These studies culminated in the identification of anthranilimides 16 and 22 which displayed potent in vitro inhibition of GPa in