66673-40-3 | (R)-(-)-5-(Hydroxymethyl)-2-pyrrolidinone

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$12.00	$9.00
10g	98%	in stock	$20.00	$14.00
25g	98%	in stock	$47.00	$33.00

Description

• Catalog Number: AB69317
• Chemical Name: (R)-(-)-5-(Hydroxymethyl)-2-pyrrolidinone
• CAS Number: 66673-40-3
• Molecular Formula: C5H9NO2
• Molecular Weight: 115.13045999999999
• MDL Number: MFCD00077791
• SMILES: OC[C@H]1CCC(=O)N1

Computed Properties

• Complexity: 103
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• Undefined Atom Stereocenter Count: 1
• XLogP3: -1

Upstream Synthesis Route

The (R)-(-)-5-(Hydroxymethyl)-2-pyrrolidinone is a vital chemical compound used in various chemical synthesis processes. This compound plays a crucial role as a building block in the creation of complex structures and functional materials. Its unique properties make it a versatile and valuable tool for chemists in organic chemistry and material science.In chemical synthesis, (R)-(-)-5-(Hydroxymethyl)-2-pyrrolidinone serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Its reactive hydroxymethyl group allows for selective modification, enabling the introduction of specific functional groups to the molecule. This flexibility makes it a sought-after reagent in the development of new compounds with targeted properties.Furthermore, (R)-(-)-5-(Hydroxymethyl)-2-pyrrolidinone can participate in various transformations such as nucleophilic additions, condensation reactions, and ring-forming processes. Its presence in a synthetic pathway can lead to efficient and high-yielding routes to intricate molecular structures. Chemists leverage its reactivity and stereochemical properties to control the outcome of reactions and enhance the overall efficiency of the synthesis.Overall, (R)-(-)-5-(Hydroxymethyl)-2-pyrrolidinone holds significant importance in chemical synthesis due to its functional versatility, reactivity, and role as a crucial building block in creating novel chemical entities. Its tailored application in diverse synthetic strategies underscores its value in the realm of modern organic chemistry.