(2R)-1-methyl-2-Piperidinecarboxylic acid

Name: (2R)-1-methyl-2-Piperidinecarboxylic acid
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CAS No. 41447-17-0
Cat. No. CS-0030802
Molecule weightNone
Purity≥97%
MDL No.MFCD13183995

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(2R)-1-methyl-2-Piperidinecarboxylic acid|CS-0030802

Structure of 41447-17-0

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General Information

CAS No. 41447-17-0
Cat. No. CS-0030802
Purity ≥97%
MDL No. MFCD13183995
Storage Store at room temperature
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₇H₁₃NO₂
Molecular Weight None
Synonym(s) (R)-1-Methylpiperidine-2-carboxylic acid
SMILES O=C(O)[C@@H]1N(CCCC1)C

Description

(2R)-1-methyl-2-piperidinecarboxylic acid features a chiral piperidine scaffold with a methylated nitrogen and carboxylic acid at the 2-position, enabling precise stereochemical control in peptide-based drug design. This bench-stable derivative integrates readily into peptidomimetic architectures, offering enhanced metabolic stability and improved membrane permeability compared to linear analogs.

Application

(2R)-1-Methyl-2-piperidinecarboxylic acid serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of bioactive molecules through established amide and ester transformations. Its stereochemical purity supports consistent biological activity in target-directed libraries. The piperidine core provides favorable pharmacokinetic properties, while the carboxylic acid functionality facilitates conjugation via standard coupling reactions. Bench-stable and readily purified by recrystallization, it functions effectively in both small-scale screening and process development workflows.

Safety Information

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Computational Chemistry Data

TPSA 40.54
LogP 0.5553
H_Acceptors 2
H_Donors 1
Rotatable_Bonds 1

Other Classifications

Building Blocks Skeleton Aliphatic heterocycle compounds Piperidine compounds

Building Blocks Skeleton Chiral compounds Chiral Building Blocks

Key Words

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(2R)-1-methyl-2-Piperidinecarboxylic acid

CAS No. 41447-17-0

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