1007462-48-7 | 2-(1,3,5-Trimethyl-1h-pyrazol-4-yl)-ethanol

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$90.00	$63.00
250mg	95%	in stock	$133.00	$93.00
1g	95%	in stock	$383.00	$268.00

Description

• Catalog Number: AA03379
• Chemical Name: 2-(1,3,5-Trimethyl-1h-pyrazol-4-yl)-ethanol
• CAS Number: 1007462-48-7
• Molecular Formula: C8H14N2O
• Molecular Weight: 154.2096
• MDL Number: MFCD08060042
• SMILES: OCCc1c(C)nn(c1C)C

Computed Properties

• Complexity: 129
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 0.6

Upstream Synthesis Route

2-(1,3,5-Trimethyl-1H-pyrazol-4-yl)ethanol, also known as $name$, serves as a versatile building block in chemical synthesis. This compound plays a crucial role as a reagent in organic reactions due to its unique structural properties. Its functional group containing the pyrazole ring enables it to participate in various transformative processes, making it a valuable tool for synthetic chemists.In chemical synthesis, $name$ can act as a nucleophile, allowing it to react with electrophiles to form new carbon-carbon or carbon-heteroatom bonds. This reactivity facilitates the creation of complex molecular structures with specific functionalities. Moreover, the trimethyl substituents on the pyrazole ring enhance the compound's stability and influence its selectivity in reactions.Additionally, the hydroxyl group present in 2-(1,3,5-Trimethyl-1H-pyrazol-4-yl)ethanol provides opportunities for further derivatization, enabling the introduction of additional functional groups to tailor the compound for specific applications. Overall, the strategic incorporation of $name$ in chemical synthesis enables the efficient construction of diverse organic molecules with tailored properties and functionalities.