(S)-N-tert-Butyldecahydroisoquinoline-3-carboxamide TCI B3410

Chemical Identity

CAS No.: 136465-81-1
PubChem: CID 454736·SID 87561092
Formula: C14H26N2O
Molecular weight: 238.37 g/mol
Purity: >97.0%(GC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (3S,4aS,8aS)-N-tert-butyl-1,2,3,4,4a,5,6,7,8,8a-decahydroisoquinoline-3-carboxamide
SMILES: CC(C)(C)NC(=O)[C@@H]1C[C@@H]2CCCC[C@@H]2CN1
InChIKey: UPZBXVBPICTBDP-TUAOUCFPSA-N

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(S)-N-tert-Butyldecahydroisoquinoline-3-carboxamide is a chiral building block used in asymmetric synthesis to construct complex molecular structures. This compound plays a critical role in chemical laboratories by enabling the formation of molecules with specific spatial configurations. Its unique chiral properties make it essential for creating enantiomerically pure compounds, which are vital in pharmaceutical and organic chemistry research. The compound is widely utilized in the development of new drugs and specialized chemical materials due to its ability to participate in stereoselective reactions.

The compound's chiral nature and molecular complexity make it a preferred choice for researchers seeking precise control over stereochemistry. Its ability to act as a substrate or intermediate in asymmetric reactions allows for the synthesis of compounds with defined stereochemical features. This makes it highly valuable in applications where the spatial arrangement of atoms significantly affects the biological activity or chemical behavior of the final product. The compound's stability and reactivity under controlled conditions further enhance its appeal in laboratory settings.

In Indonesian laboratories, this compound is commonly used by chemists and pharmacologists working on drug development and organic synthesis projects. Its role in creating chiral molecules with specific biological activities is crucial for advancing research in medicinal chemistry. The compound's versatility and reliability make it a key component in the toolkit of researchers focused on asymmetric synthesis. Its application is particularly relevant in studies requiring high stereoselectivity and precision in molecular construction.

TCI brochures (PDF)

Chiral Building Blocks 2025-04-14 · p. 5

Related TCI products

Asymmetric Synthesis: This compound is ideal for creating enantiomerically pure compounds, essential in pharmaceutical research for drug development.
Chiral Compound Development: Its chiral structure enables the synthesis of complex molecules with specific stereochemical configurations.
Organic Chemistry Research: It supports the creation of organic compounds with defined spatial arrangements, enhancing the accuracy of chemical reactions.
Drug Discovery: The compound is used to develop new drugs with precise stereochemical properties, improving their efficacy and safety.
Stereocontrolled Reactions: It provides the necessary chiral environment for reactions requiring strict control over stereochemistry.

Brand	TCI
CAS number	136465-81-1
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid
Storage	Store in a cool, dry place away from light

This compound should be stored in a cool, dry environment, away from direct light and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chiral nature, it should be handled with care to maintain its stereochemical integrity during synthesis processes. Proper labeling and storage conditions are essential to ensure its stability and usability in laboratory applications. Always follow standard safety protocols when handling chemical substances to minimize risks and ensure a safe working environment.

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