4492-02-8 | Ethyl 4,5,6,7-tetrahydro-1H-indazole-3-carboxylate

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$5.00	$4.00
250mg	98%	in stock	$7.00	$5.00
1g	98%	in stock	$17.00	$12.00
5g	98%	in stock	$69.00	$49.00
10g	98%	in stock	$137.00	$96.00
25g	98%	in stock	$276.00	$194.00

Description

• Catalog Number: AG16834
• Chemical Name: Ethyl 4,5,6,7-tetrahydro-1H-indazole-3-carboxylate
• CAS Number: 4492-02-8
• Molecular Formula: C10H14N2O2
• Molecular Weight: 194.23036000000005
• MDL Number: MFCD02942367
• SMILES: CCOC(=O)c1n[nH]c2c1CCCC2

Computed Properties

• Complexity: 220
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 2

Upstream Synthesis Route

Ethyl 4,5,6,7-tetrahydro-1H-indazole-3-carboxylate, also known as $name$, is a versatile compound frequently utilized in chemical synthesis due to its unique properties. This compound serves as a valuable building block in the creation of various organic molecules, particularly in the pharmaceutical and agrochemical industries.In chemical synthesis, $name$ can undergo a range of reactions, such as esterification, hydrolysis, and reduction, to yield structurally diverse derivatives with potential biological activities. Its indazole moiety provides a reactive site for functionalization, allowing for the introduction of different substituents to modulate the compound's properties.Researchers often employ $name$ as a key intermediate in the production of novel drug candidates or innovative agrochemicals. By incorporating this compound into their synthetic routes, chemists can access a plethora of molecular scaffolds that exhibit promising pharmacological or pesticidal effects.Moreover, the strategic placement of the carboxylate ester group in $name$ enables precise manipulation of its chemical reactivity, facilitating the construction of complex molecular frameworks in a controlled manner. This feature makes $name$ a valuable tool for designing and synthesizing target compounds with specific biological functions or structural motifs.Overall, the application of Ethyl 4,5,6,7-tetrahydro-1H-indazole-3-carboxylate in chemical synthesis is fundamental to the development of novel molecules with diverse applications in the realm of pharmaceuticals and agrochemicals. Its versatility and reactivity make it an indispensable building block for organic chemists seeking to create innovative and functionalized compounds for various industries.

Literature

• Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

  Bioorganic & medicinal chemistry letters 20101101