193086-04-3

Basic information

• Product Name: {1,1-dimethyl-2-[(methyl-{1-[methyl-(1-methylcarbamoyl-2-phenyl-ethyl)-carbamoyl]-2-naphthalen-2-yl-ethyl}-carbamoyl)-methoxy]-ethyl}-carbamic acid tert-butyl ester
• Synonyms: {1,1-dimethyl-2-[(methyl-{1-[methyl-(1-methylcarbamoyl-2-phenyl-ethyl)-carbamoyl]-2-naphthalen-2-yl-ethyl}-carbamoyl)-methoxy]-ethyl}-carbamic acid tert-butyl ester
• CAS NO: 193086-04-3
• Molecular Weight: 632.8
• Mol File: 193086-04-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: {1,1-dimethyl-2-[(methyl-{1-[methyl-(1-methylcarbamoyl-2-phenyl-ethyl)-carbamoyl]-2-naphthalen-2-yl-ethyl}-carbamoyl)-methoxy]-ethyl}-carbamic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: {1,1-dimethyl-2-[(methyl-{1-[methyl-(1-methylcarbamoyl-2-phenyl-ethyl)-carbamoyl]-2-naphthalen-2-yl-ethyl}-carbamoyl)-methoxy]-ethyl}-carbamic acid tert-butyl ester(193086-04-3)
• EPA Substance Registry System: {1,1-dimethyl-2-[(methyl-{1-[methyl-(1-methylcarbamoyl-2-phenyl-ethyl)-carbamoyl]-2-naphthalen-2-yl-ethyl}-carbamoyl)-methoxy]-ethyl}-carbamic acid tert-butyl ester(193086-04-3)

Safety Data

• Hazardous Substances Data: 193086-04-3(Hazardous Substances Data)

Upstream product

• 186840-95-9 (2R)-N-Methyl-2-methylamino-N-((1R)-1-(methylcarbamoyl)-2-phenylethyl)-3-(2-naphthyl)propionamide 
• 193085-32-4 (2-tert-butoxycarbonylamino-2-methylpropoxy)acetic acid 
• 249762-00-3 (2-tert-butoxycarbonylamino-2-methyl-propoxy)-acetic acid ethyl ester 
• 102520-97-8 2-((tert-butyloxycarbonyl)amino)-2-methylpropan-1-ol 

Relevant articles and documents

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.