108233-37-0 | Boc-nva-osu

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$74.00	$52.00
5g	97%	in stock	$203.00	$142.00
25g	97%	in stock	$573.00	$402.00
100g	97%	in stock	$1,536.00	$1,075.00

Description

• Catalog Number: AI07353
• Chemical Name: Boc-nva-osu
• CAS Number: 108233-37-0
• Molecular Formula: C14H22N2O6
• Molecular Weight: 314.3343
• MDL Number: MFCD01862291
• SMILES: CCC[C@@H](C(=O)ON1C(=O)CCC1=O)NC(=O)OC(C)(C)C

Computed Properties

• Complexity: 452
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 22
• Hydrogen Bond Acceptor Count: 6
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 8
• XLogP3: 1.2

Upstream Synthesis Route

Carbamic acid, [(1S)-1-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]butyl]-, 1,1-dimethylethyl ester is a versatile compound commonly utilized in chemical synthesis. This compound is valued for its ability to act as a key building block in the creation of various complex organic molecules. In particular, it is frequently employed as a precursor in the synthesis of pharmaceutical ingredients, agrochemicals, and specialty chemicals.Due to its unique chemical structure, Carbamic acid, [(1S)-1-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]butyl]-, 1,1-dimethylethyl ester can undergo various chemical reactions, including acylation, amidation, and esterification. These reactions allow for the modification and functionalization of the compound, enabling chemists to tailor its properties for specific applications. Additionally, the presence of the butyl and pyrrolidinyl moieties in the molecule provides opportunities for diversifying the molecular structure and introducing chirality, which is crucial in the synthesis of chiral compounds.Overall, Carbamic acid, [(1S)-1-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]butyl]-, 1,1-dimethylethyl ester serves as a valuable intermediate in the synthesis of intricate organic molecules with diverse applications in the fields of pharmaceuticals, agrochemicals, and specialty chemicals. Its versatility and reactivity make it an indispensable tool for chemists engaged in the development of novel compounds and materials.