152120-54-2 | N,N'-Di-Boc-1h-pyrazole-1-carboxamidine

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$9.00	$6.00
5g	98%	in stock	$10.00	$7.00
10g	98%	in stock	$15.00	$10.00
25g	98%	in stock	$29.00	$20.00
50g	98%	in stock	$56.00	$39.00
100g	98%	in stock	$110.00	$77.00

Description

• Catalog Number: AB46645
• Chemical Name: N,N'-Di-Boc-1h-pyrazole-1-carboxamidine
• CAS Number: 152120-54-2
• Molecular Formula: C14H22N4O4
• Molecular Weight: 310.3489
• MDL Number: MFCD01075122
• SMILES: O=C(OC(C)(C)C)NC(=NC(=O)OC(C)(C)C)n1cccn1

Computed Properties

• Complexity: 449
• Covalently-Bonded Unit Count: 1
• Defined Bond Stereocenter Count: 1
• Heavy Atom Count: 22
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 6
• XLogP3: 3.1

Upstream Synthesis Route

N,N-Bis-Boc-1-Guanylpyrazole is a versatile compound commonly utilized in chemical synthesis as a versatile building block. It serves as an efficient precursor for the introduction of guanidine functionalities into organic molecules, making it valuable in medicinal chemistry, materials science, and catalysis.In chemical synthesis, N,N-Bis-Boc-1-Guanylpyrazole is often employed as a guanidine synthon, enabling the selective incorporation of guanidine moieties into complex molecules. This compound's reactivity allows for the preparation of a wide range of guanidine derivatives, which are pivotal in the development of pharmaceuticals, agrochemicals, and functional materials.Furthermore, N,N-Bis-Boc-1-Guanylpyrazole exhibits unique properties that make it a preferred reagent in organic transformations. Its stability, ease of handling, and compatibility with various reaction conditions make it a go-to choice for chemists looking to introduce guanidine functionalities with precision and efficiency.Overall, the application of N,N-Bis-Boc-1-Guanylpyrazole in chemical synthesis offers researchers a powerful tool to access diverse guanidine-containing compounds with tailored properties, paving the way for innovative advancements in the field of organic chemistry.