97482-27-4

Basic information

• Product Name: 1H-Pyrrolo[1,2-c]imidazol-1-one,hexahydro-3,3-dimethyl-,(S)-(9CI)
• Synonyms: 1H-Pyrrolo[1,2-c]imidazol-1-one,hexahydro-3,3-dimethyl-,(S)-(9CI)
• CAS NO: 97482-27-4
• Molecular Formula: C₈H₁₄N₂O
• Molecular Weight: 0
• Product Categories: PYRROLE
• Mol File: 97482-27-4.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-Pyrrolo[1,2-c]imidazol-1-one,hexahydro-3,3-dimethyl-,(S)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrolo[1,2-c]imidazol-1-one,hexahydro-3,3-dimethyl-,(S)-(9CI)(97482-27-4)
• EPA Substance Registry System: 1H-Pyrrolo[1,2-c]imidazol-1-one,hexahydro-3,3-dimethyl-,(S)-(9CI)(97482-27-4)

Safety Data

• Hazardous Substances Data: 97482-27-4(Hazardous Substances Data)

Usage

General Description

1H-Pyrrolo[1,2-c]imidazol-1-one, hexahydro-3,3-dimethyl-,(S)-(9CI) is a chemical compound that is a derivative of pyrrolo[1,2-c]imidazole. It is a white, crystalline solid with the molecular formula C9H14N2O. 1H-Pyrrolo[1,2-c]imidazol-1-one,hexahydro-3,3-dimethyl-,(S)-(9CI) is chiral and exists in the (S)-enantiomeric form. It is commonly used as a building block in organic synthesis, particularly in the pharmaceutical industry for the production of various biologically active molecules. Additionally, it has been studied for its potential biological activities and pharmacological properties, making it an important compound in medicinal chemistry and drug development.

Upstream product

• 67-64-1 acetone 
• 7531-52-4 L-prolinamide 

Downstream Products

• 185736-59-8 (4R,5S,6S)-3-[2-((S)-3,3-Dimethyl-1-oxo-tetrahydro-pyrrolo[1,2-c]imidazol-2-yl)-ethylsulfanyl]-6-((R)-1-hydroxy-ethyl)-4-methyl-7-oxo-1-aza-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid 4-nitro-benzyl ester 
• 174089-62-4 (2S)-N-propan-2-ylpyrrolidine-2-carboxamide 
• 7531-52-4 L-prolinamide 
• 185736-39-4 (5S)-2,2-dimethyl-3-(2-p-toluenesulfonyloxyethyl)-1,3-diazabicyclo[3.3.0]octan-4-one 

Relevant articles and documents

The role of Zn2+ in enhancing the rate and stereoselectivity of the aldol reactions catalyzed by the simple prolinamide model

The aldol reaction between acetone and 4-nitrobenzaldehyde catalyzed by single l-prolinamide and its zinc complexes has been studied. An increase in the rate and the stereoselectivity of the reaction has been shown by using zinc derivatives. A mechanistic

Synthesis and antibacterial activity of 1-β-methylcarbapenem having a 1,3-diazabicyclo[3.3.0]octan-4-one moiety

The synthesis of new series of 1-β-methylcarbapenems having a 1,3-diazabicyclo[3.3.0]octan-4-one moiety is described. Their in vitro antibacterial activities against both Gram-positive and Gram negative bacteria are reported and the effect of the substituent on the bicyclic ring was investigated and was in agreement with findings from our previous studies.