274-47-5 | Imidazo[1,5-a]pyridine

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$15.00	$11.00
5g	98%	in stock	$59.00	$42.00
10g	98%	in stock	$118.00	$83.00
25g	98%	in stock	$228.00	$160.00

Description

• Catalog Number: AD53431
• Chemical Name: Imidazo[1,5-a]pyridine
• CAS Number: 274-47-5
• Molecular Formula: C7H6N2
• Molecular Weight: 118.1359
• MDL Number: MFCD03407375
• SMILES: c1ccc2n(c1)cnc2
• NSC Number: 119858

Computed Properties

• Complexity: 103
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 1
• XLogP3: 1.8

Literature

• Synthesis, characterization, optical properties and theoretical studies of novel substituted imidazo[1,5-a]pyridinyl 1,3,4-oxadiazole derivatives.

  Journal of fluorescence 20121101

• Fluorescence switching of imidazo[1,5-a]pyridinium ions: pH-sensors with dual emission pathways.

  Organic letters 20120615

• Studies toward the total synthesis of nagelamide K.

  Organic letters 20120420

• Efficient, single-step access to imidazo[1,5-a]pyridine n-heterocyclic carbene precursors.

  Organic letters 20111007

• Multicomponent reaction of imidazo[1,5-a]pyridine carbenes with aldehydes and dimethyl acetylenedicarboxylate or allenoates: a straightforward approach to fully substituted furans.

  The Journal of organic chemistry 20101001

• Orthogonal synthesis of densely functionalized pyrroles and thiophenes from the reactions of imidazo[1,5-a]pyridine carbene-derived zwitterions with electron-deficient alkynes.

  The Journal of organic chemistry 20100402

• Pyrido[1,2-a][1,2,4]triazol-3-ylidenes as a new family of stable annulated N-heterocyclic carbenes: synthesis, reactivity, and their application in coordination chemistry and organocatalysis.

  The Journal of organic chemistry 20081107

• Synthesis of 2-azaindolizines by using an iodine-mediated oxidative desulfurization promoted cyclization of N-2-pyridylmethyl thioamides and an investigation of their photophysical properties.

  Organic letters 20061123

• Imidazo[1,5-a]pyridine: a versatile architecture for stable N-heterocyclic carbenes.

  Journal of the American Chemical Society 20050316