887245-67-2

Usage

Uses

Used in Pharmaceutical Industry:
Cyclohexanecarboxylic acid, 1-amino-4-oxo-, methyl ester is used as a precursor in the synthesis of various drugs for its ability to contribute to the formation of complex molecular structures. Its presence in drug development allows for the creation of new therapeutic agents with potential medicinal properties.
Used in Organic Chemistry Reactions:
In the realm of organic chemistry, Cyclohexanecarboxylic acid, 1-amino-4-oxo-, methyl ester is employed as a building block for constructing more complex organic molecules. Its diverse functional groups enable it to participate in a wide range of chemical reactions, making it a valuable component in the synthesis of various organic compounds.
It is crucial to handle Cyclohexanecarboxylic acid, 1-amino-4-oxo-, methyl ester with care, as it may present health risks if not managed properly. Proper safety measures should be taken to mitigate any potential hazards associated with its use.

Upstream product

• 67-56-1 methanol 
• 54621-18-0 8-amino-1,4-dioxa-spiro[4.5]decane-8-carboxylic acid 
• 191111-27-0 methyl 1-((tert-butoxycarbonyl)amino)-4-oxocyclohexanecarboxylate 

Downstream Products

• 917887-37-7 1-[N-(trifluoroacetyl)amino]-4-cyclohexanon-1-carboxylic acid methyl ester 
• 887245-68-3 C₁₉H₂₀N₂O₄ 
• 331258-40-3 methyl 1-benzimido-4-oxocyclohexane-1-carboxylate 
• 917887-36-6 1-[N-(phthaloyl)amino]-4-cyclohexanon-1-carboxylic acid methyl ester 

Relevant academic research and scientific papers

PROCESS FOR PREPARING SUBSTITUTED CYCLOHEXANE AMINO ACID ESTERS AND SPIROKETAL-SUBSTITUTED CYCLIC KETO-ENOLS

The present invention relates to a novel process for preparing substituted cyclohexane amino acid esters and spiroketal-substituted cyclic keto-enols, and to novel intermediates or starting compounds that are passed through or used in the process according to the invention.

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

Stereoselective Synthesis of Amino Acid Analogs for Tumor Imaging

The radiolabeled non-natural amino acid 1-amino-3-cyclobutane-1-carboxylic acid (ACBC) and its analogs are candidate tumor imaging agents useful for positron emission tomography and single photon emission computed tomography due to their selective affinity for tumor cells. The present invention provides methods for stereo-selective synthesis of syn-ACBC analogs. The disclosed synthetic strategy is reliable and efficient and can be used to synthesize a gram quantity of various syn-isomers of the ACBC analogs, particularly, syn-[18F]-1-amino-3-fluorocyclobutane-1-carboxylic acid (FACBC) and syn-[123I]-1-amino-3-iodocyclobutane-1-carboxylic (IACBC) acid analogs.