1107620-72-3 | tert-Butyl N-(1H-pyrazol-4-ylmethyl)carbamate

Packsize	Purity	Availability	Price	Discounted Price
100mg	≥98%	in stock	$65.00	$45.00
250mg	≥98%	in stock	$93.00	$65.00
1g	≥98%	in stock	$172.00	$120.00
5g	≥98%	in stock	$512.00	$358.00
10g	≥98%	in stock	$786.00	$550.00
25g	≥98%	in stock	$1,372.00	$960.00
100g	≥98%	in stock	$5,429.00	$3,800.00

Description

• Catalog Number: AB65918
• Chemical Name: tert-Butyl N-(1H-pyrazol-4-ylmethyl)carbamate
• CAS Number: 1107620-72-3
• Molecular Formula: C9H15N3O2
• Molecular Weight: 197.2343
• MDL Number: MFCD12820298
• SMILES: O=C(OC(C)(C)C)NCc1c[nH]nc1

Computed Properties

• Complexity: 201
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 4
• XLogP3: 0.7

Upstream Synthesis Route

4-(Boc-aminomethyl)pyrazole is a valuable building block in chemical synthesis, widely utilized for its versatility and reactivity. This compound plays a crucial role in organic synthesis due to its unique structure and functional groups. With the Boc (tert-butoxycarbonyl) protecting group at the amino moiety, 4-(Boc-aminomethyl)pyrazole serves as an excellent intermediate for the preparation of various pharmaceuticals, agrochemicals, and bioactive compounds.One application of 4-(Boc-aminomethyl)pyrazole is in the synthesis of peptide analogs and peptidomimetics. The Boc protecting group allows for selective deprotection under mild conditions, enabling the controlled manipulation of the amino functionality. By incorporating 4-(Boc-aminomethyl)pyrazole into peptide synthesis, chemists can access a diverse array of modified peptides with enhanced stability and biological activity.Furthermore, 4-(Boc-aminomethyl)pyrazole can be used in the construction of heterocyclic compounds through cyclization reactions. Its pyrazole ring system offers opportunities for further functionalization and scaffold diversification, making it a valuable tool in medicinal chemistry and drug discovery efforts. Additionally, the Boc protecting group provides stability during synthetic transformations, ensuring the preservation of the key functionalities required for subsequent reactions.Overall, the strategic incorporation of 4-(Boc-aminomethyl)pyrazole in chemical synthesis facilitates the efficient assembly of complex molecules with tailored properties and biological functions. Its versatility and compatibility with diverse synthetic strategies make it a valuable asset for researchers and chemists working in the fields of organic chemistry and medicinal chemistry.