(R)-(-)-2-Methylpiperazine TCI M2091

Chemical Identity

CAS No.: 75336-86-6
PubChem: CID 7330434·SID 87561459
Formula: C5H12N2
Molecular weight: 100.16 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2R)-2-methylpiperazine
SMILES: C[C@@H]1CNCCN1
InChIKey: JOMNTHCQHJPVAZ-RXMQYKEDSA-N

Rp 1.140.300,00

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Berat 5g

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(R)-(-)-2-Methylpiperazine is a chiral compound widely used in asymmetric synthesis to construct complex molecular structures. This chemical plays a crucial role in laboratories where precise control over stereochemistry is essential. Its unique chiral configuration allows it to act as a building block in the development of pharmaceuticals and organic chemicals. As a key reagent in synthetic pathways, it supports the creation of enantiomerically pure compounds, which are vital in drug development and advanced chemical research.

The compound's stability under specific conditions and its ability to participate in nucleophilic and substitution reactions make it a preferred choice for chemists. Its chiral nature ensures that it can selectively influence reaction outcomes, enhancing the efficiency of synthetic processes. Additionally, its solid form and compatibility with various reagents make it versatile for use in a range of experimental setups. These properties contribute to its widespread application in both academic and industrial research environments.

In Indonesian laboratories, (R)-(-)-2-Methylpiperazine is commonly used in organic chemistry, pharmacology, and the synthesis of bioactive compounds. Its role in controlling stereochimical outcomes is particularly important in research focused on drug development and advanced chemical synthesis. The compound’s availability and reliability make it a valuable asset in scientific investigations requiring precise stereochemical control.

TCI brochures (PDF)

Chiral Building Blocks 2025-04-14 · p. 4

Related TCI products

Organic chemistry research benefits from this compound's role in constructing complex molecular frameworks with controlled stereochemistry.
Pharmaceutical development utilizes its chiral properties to synthesize enantiomerically pure compounds essential for drug efficacy.
Bioactive compound synthesis relies on its ability to participate in nucleophilic and substitution reactions, enhancing synthetic versatility.
Academic research in asymmetric synthesis leverages its unique chiral configuration for precise stereochemical control.
Industrial chemical production incorporates it as a key reagent in the creation of specialized organic compounds with specific stereochemical profiles.

Brand	TCI
CAS number	75336-86-6
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	—
Physical form	Solid
Storage	Store in a cool, dry place away from light

This compound should be stored in a cool, dry place away from direct light to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chiral nature, it is important to handle it with care to avoid any unintended stereochemical changes. Proper labeling of containers is essential for safe handling and to prevent mix-ups in the laboratory. Always ensure that the workspace is clean and free from potential reactive substances. When working with this material, it is advisable to use appropriate personal protective equipment to ensure safety during handling and experimentation.

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