59646-16-1 | 5H,6H,7H-Pyrrolo[1,2-a]imidazole

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$8.00	$6.00
250mg	98%	in stock	$15.00	$11.00

Description

• Catalog Number: AG69482
• Chemical Name: 5H,6H,7H-Pyrrolo[1,2-a]imidazole
• CAS Number: 59646-16-1
• Molecular Formula: C6H8N2
• Molecular Weight: 108.14111999999999
• MDL Number: MFCD11870771
• SMILES: C1Cn2c(C1)ncc2

Computed Properties

• Complexity: 92.5
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 1
• Undefined Atom Stereocenter Count: 1
• XLogP3: 0.4

Upstream Synthesis Route

5H-Pyrrolo[1,2-a]imidazole, 6,7-dihydro- is a versatile compound widely used in organic synthesis as a building block for various advanced materials and pharmaceuticals. Its unique structure makes it a valuable precursor for the synthesis of complex molecules with potential biological activities. In chemical synthesis, this compound can serve as a key intermediate in the preparation of heterocyclic compounds, which are essential in the design and development of drugs, agrochemicals, and functional materials. Its reactivity allows for the formation of diverse chemical bonds, enabling the construction of complex molecular frameworks efficiently.Researchers often utilize 5H-Pyrrolo[1,2-a]imidazole, 6,7-dihydro- as a versatile starting material to access a wide range of compounds with tailored properties. Its incorporation in synthetic pathways can lead to the creation of novel molecules with enhanced biological or physicochemical characteristics, opening up new possibilities for applications in various fields of chemistry.Overall, the use of 5H-Pyrrolo[1,2-a]imidazole, 6,7-dihydro- in chemical synthesis plays a crucial role in expanding the realm of molecular design and discovery, offering valuable opportunities for the development of innovative materials and pharmaceuticals.

Literature

• H2O2 production downstream of FLT3 is mediated by p22phox in the endoplasmic reticulum and is required for STAT5 signalling.

  PloS one 20120101

• Neurotoxic factors released by stimulated human monocytes and THP-1 cells.

  Brain research 20110711

• Chiral bicycle imidazole nucleophilic catalysts: rational design, facile synthesis, and successful application in asymmetric Steglich rearrangement.

  Journal of the American Chemical Society 20101117

• The neuroprotective action of JNK3 inhibitors based on the 6,7-dihydro-5H-pyrrolo[1,2-a]imidazole scaffold.

  Bioorganic & medicinal chemistry letters 20051101