92525-10-5 | 3-Iodo-1-methyl-1H-pyrazole

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$6.00	$4.00
250mg	97%	in stock	$7.00	$5.00
1g	97%	in stock	$18.00	$13.00
5g	97%	in stock	$40.00	$28.00
10g	97%	in stock	$65.00	$45.00
25g	97%	in stock	$148.00	$103.00

Description

• Catalog Number: AB48509
• Chemical Name: 3-Iodo-1-methyl-1H-pyrazole
• CAS Number: 92525-10-5
• Molecular Formula: C4H5IN2
• Molecular Weight: 208.0004
• MDL Number: MFCD28505600
• SMILES: Cn1ccc(n1)I

Computed Properties

• Complexity: 66.7
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 7
• Hydrogen Bond Acceptor Count: 1
• XLogP3: 0.9

Upstream Synthesis Route

3-Iodo-1-methyl-1H-pyrazole is a versatile compound widely utilized in chemical synthesis for its unique reactivity and functional group compatibility. This compound serves as a valuable building block in the preparation of various advanced organic molecules through a range of synthetic transformations. 1. Cross-Coupling Reactions: 3-Iodo-1-methyl-1H-pyrazole is an excellent substrate for palladium-catalyzed cross-coupling reactions, enabling the construction of complex structures such as biaryls, heterocycles, and natural product derivatives.2. Functional Group Interconversion: Due to the presence of the iodo group, 3-Iodo-1-methyl-1H-pyrazole can participate in diverse functional group interconversion reactions, facilitating the introduction of different moieties for further modification.3. Nucleophilic Substitution: The presence of the iodo substituent in 3-Iodo-1-methyl-1H-pyrazole makes it a suitable candidate for nucleophilic substitution reactions, allowing for the easy introduction of various nucleophiles to generate diverse chemical scaffolds.Overall, 3-Iodo-1-methyl-1H-pyrazole plays a crucial role in modern organic synthesis by enabling the efficient construction of structurally complex and diverse molecules with potential applications in pharmaceuticals, materials science, and agrochemicals.