1153950-54-9 | (R)-Pyrrolidine-3-carbonitrile hydrochloride

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$36.00	$26.00
250mg	95%	in stock	$88.00	$62.00
500mg	95%	in stock	$176.00	$124.00
1g	95%	in stock	$278.00	$195.00
5g	95%	in stock	$835.00	$584.00

Description

• Catalog Number: AA20414
• Chemical Name: (R)-Pyrrolidine-3-carbonitrile hydrochloride
• CAS Number: 1153950-54-9
• Molecular Formula: C5H9ClN2
• Molecular Weight: 132.59136
• MDL Number: MFCD11656839
• SMILES: N#C[C@H]1CNCC1.Cl

Computed Properties

• Complexity: 99.9
• Covalently-Bonded Unit Count: 2
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2

Upstream Synthesis Route

The (R)-Pyrrolidine-3-carbonitrile hydrochloride is a versatile chemical compound widely used in chemical synthesis processes. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its chirality, stemming from its (R)-configuration, is crucial in determining the stereochemistry of the products obtained in asymmetric synthesis.In organic chemistry, (R)-Pyrrolidine-3-carbonitrile hydrochloride is often employed as a key intermediate in the synthesis of complex molecules. Its unique structure and reactivity make it an essential component in the creation of a diverse range of compounds. By utilizing this compound, chemists can efficiently introduce the pyrrolidine ring and the cyano group into their target molecules, enabling the synthesis of intricate structures with high precision.Furthermore, the (R)-Pyrrolidine-3-carbonitrile hydrochloride can participate in various types of chemical reactions, including nucleophilic additions, substitution reactions, and asymmetric transformations. Its compatibility with different reaction conditions and functional groups make it a valuable tool for synthetic chemists seeking to construct molecules with specific stereochemistry and functionalities.Overall, the (R)-Pyrrolidine-3-carbonitrile hydrochloride plays a crucial role in advancing chemical synthesis by enabling the efficient construction of complex molecules with high stereochemical control and functional diversity. Its applications extend across various industries, including pharmaceuticals, agrochemicals, and materials science, making it a valuable compound in the field of organic chemistry.