119838-38-9 | (S)-tert-Butyl 2-(tert-butyl)-3-methyl-4-oxoimidazolidine-1-carboxylate

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$47.00	$33.00
250mg	95%	in stock	$114.00	$80.00
1g	95%	in stock	$266.00	$187.00
5g	95%	in stock	$681.00	$477.00

Description

• Catalog Number: AA33185
• Chemical Name: (S)-tert-Butyl 2-(tert-butyl)-3-methyl-4-oxoimidazolidine-1-carboxylate
• CAS Number: 119838-38-9
• Molecular Formula: C13H24N2O3
• Molecular Weight: 256.3413
• MDL Number: MFCD00075101
• SMILES: O=C(N1CC(=O)N([C@@H]1C(C)(C)C)C)OC(C)(C)C

Computed Properties

• Complexity: 352
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 18
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• XLogP3: 2.3

Upstream Synthesis Route

(S)-(-)-1-Boc-2-tert-butyl-3-methyl-4-imidazolidinone is a valuable chiral building block widely used in chemical synthesis. Its unique structure and chirality make it a versatile tool for asymmetric transformations and the synthesis of complex organic molecules. In particular, this compound is utilized as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its Boc (tert-butoxycarbonyl) protection group can be selectively removed under mild conditions, allowing for further functionalization at the nitrogen atom. Additionally, the tert-butyl and methyl substituents on the imidazolidinone ring provide steric hindrance that is crucial for controlling diastereoselectivity in organic reactions. Overall, (S)-(-)-1-Boc-2-tert-butyl-3-methyl-4-imidazolidinone plays a pivotal role in modern organic synthesis, enabling chemists to access enantiomerically pure compounds with high selectivity and efficiency.