6967-12-0 | 6-Aminoindazole

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$16.00	$11.00
10g	98%	in stock	$20.00	$14.00
25g	98%	in stock	$47.00	$33.00
100g	98%	in stock	$174.00	$122.00
500g	98%	in stock	$805.00	$564.00

Description

• Catalog Number: AB69676
• Chemical Name: 6-Aminoindazole
• CAS Number: 6967-12-0
• Molecular Formula: C7H7N3
• Molecular Weight: 133.1506
• MDL Number: MFCD00005696
• SMILES: Nc1ccc2c(c1)[nH]nc2

Computed Properties

• Complexity: 126
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• XLogP3: 1.6

Upstream Synthesis Route

1H-Indazol-6-amine is a versatile compound widely utilized in chemical synthesis for its unique properties. It serves as a precursor in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. With its cyclic structure and amine functional group, 1H-Indazol-6-amine can participate in a variety of organic reactions, including nucleophilic substitutions, redox reactions, and condensation reactions. One key application of this compound is as a building block in the synthesis of heterocyclic compounds, which are essential in drug discovery and development. Additionally, 1H-Indazol-6-amine can be functionalized to introduce specific chemical functionalities, allowing for the creation of tailored molecules with desired properties. Its strategic placement in complex molecule assembly makes it a valuable tool in the hands of synthetic chemists seeking to design novel compounds with potential applications in various industries.

Literature

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  Bioorganic & medicinal chemistry 20090901

• 1H-Pyrazolo[4,3-g]benzothia-zol-7-amine.

  Acta crystallographica. Section E, Structure reports online 20090501

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  Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

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  Chemical research in toxicology 20050601

• Endothelial nitric oxide modulates perivascular sensory neurotransmission in the rat isolated mesenteric arterial bed.

  British journal of pharmacology 20020901

• Identification of novel Ah receptor agonists using a high-throughput green fluorescent protein-based recombinant cell bioassay.

  Biochemistry 20020122