21075-83-2 | 1-Boc-1-methylhydrazine

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$8.00	$5.00
10g	98%	in stock	$10.00	$7.00
25g	98%	in stock	$13.00	$10.00
50g	98%	in stock	$26.00	$18.00
100g	98%	in stock	$46.00	$32.00
500g	98%	in stock	$213.00	$150.00

Description

• Catalog Number: AB20255
• Chemical Name: 1-Boc-1-methylhydrazine
• CAS Number: 21075-83-2
• Molecular Formula: C6H14N2O2
• Molecular Weight: 146.1876
• MDL Number: MFCD05669700
• SMILES: O=C(N(N)C)OC(C)(C)C

Computed Properties

• Complexity: 128
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 0.4

Upstream Synthesis Route

1-Boc-1-methylhydrazine, also known as N-tert-butoxycarbonyl-N-methylhydrazine, serves as a versatile building block in various chemical synthesis pathways. This compound is particularly valuable in the field of organic chemistry due to its unique reactivity and functional group compatibility. In chemical synthesis, 1-Boc-1-methylhydrazine is commonly used as a protective group for amines, enabling selective reactions at specific nitrogen atoms within a molecule.By utilizing 1-Boc-1-methylhydrazine as a protecting agent, chemists can control the regioselectivity and chemoselectivity of their reactions, facilitating the synthesis of complex organic compounds with precise structural modifications. Furthermore, the tert-butoxycarbonyl (Boc) group provides stability and protection to the amine functionality, allowing for subsequent transformations without impacting the desired reaction sites.In addition to its role as a protecting group, 1-Boc-1-methylhydrazine can also participate in various organic transformations, such as nucleophilic addition reactions, condensations, and reduction processes. Its compatibility with a wide range of functional groups makes it a valuable reagent for the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.Overall, the strategic incorporation of 1-Boc-1-methylhydrazine in chemical synthesis enables chemists to access new synthetic pathways, control reaction outcomes, and ultimately accelerate the discovery and development of novel compounds with potential applications in diverse fields.