193086-00-9

Basic information

• Product Name: 2-CarboxyMethoxyMethyl-piperidine-1-carboxylic acid tert-butyl ester
• Synonyms: 2-CarboxyMethoxyMethyl-piperidine-1-carboxylic acid tert-butyl ester;2-(1-(tert-Butoxycarbonyl)piperidin-2-yl)-2-Methoxyacetic acid
• CAS NO: 193086-00-9
• Molecular Formula: C₁₃H₂₃NO₅
• Molecular Weight: 273.32542
• Mol File: 193086-00-9.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-CarboxyMethoxyMethyl-piperidine-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CarboxyMethoxyMethyl-piperidine-1-carboxylic acid tert-butyl ester(193086-00-9)
• EPA Substance Registry System: 2-CarboxyMethoxyMethyl-piperidine-1-carboxylic acid tert-butyl ester(193086-00-9)

Safety Data

• Hazardous Substances Data: 193086-00-9(Hazardous Substances Data)

Upstream product

• 193086-02-1 2-ethoxycarbonylmethoxymethyl-piperidine-1-carboxylic acid tert-butyl ester 
• 1018826-49-7 tert-butyl 2-((2-tert-butoxy-2-oxoethoxy)methyl)piperidine-1-carboxylate 
• 157634-00-9 tert-butyl 2-(hydroxymethyl)piperidine-1-carboxylate 

Downstream Products

• 193086-01-0 2-[(methyl-{1-[methyl-(1-methylcarbamoyl-2-phenyl-ethyl)-carbamoyl]-2-naphthalen-2-yl-ethyl}-carbamoyl)-methoxymethyl]-piperidine-1-carboxylic acid tert-butyl ester 

Relevant articles and documents

SUBSTITUTED SULFONAMIDE COMPOUNDS

Substituted sulfonamide derivatives, a process for their preparation, pharmaceutical compositions containing these compounds, and to the use of substituted sulfonamide derivatives in the treatment or inhibition of pain and/or various disorders or disease states.

Synthesis and in vitro characterization of new growth hormone secretagogues derived from ipamorelin with dipeptidomimetic N-terminals

The structural requirements for N-terminal features for the minimal structure of growth hormone secretagogues derived from ipamorelin are investigated. It is found, that incorporation of nonpolar peptidomimetic amino acids at the N-terminal can replace the Aib-His moiety and lead to compounds with high in vitro potency with respect to their growth hormone secretagogue properties. New unnatural amino acids with double bonds, ether- linkages, and 1,3-phenylene-moieties in the backbone proved to be valuable dipeptidomimetics. Using them, growth hormone secretagogues with high potencies were obtained.