(S,S)-(+)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediamine TCI B4647

Chemical Identity

CAS No.: 135616-36-3
PubChem: CID 135415899·SID 468590520
Formula: C36H54N2O2
Molecular weight: 546.8 g/mol
Purity: >98.0%(HPLC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2,4-ditert-butyl-6-[[(1S,2S)-2-[(3,5-ditert-butyl-2-hydroxyphenyl)methylideneamino]cyclohexyl]iminomethyl]phenol
SMILES: CC(C)(C)C1=CC(=C(C(=C1)C(C)(C)C)O)C=N[C@H]2CCCC[C@@H]2N=CC3=C(C(=CC(=C3)C(C)(C)C)C(C)(C)C)O
InChIKey: FYNXDGNCEBQLGC-KYJUHHDHSA-N

Rp 4.929.750,00

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Berat 5g 25g

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TCI B4647 135616-36-3 (S,S)-(+)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediamine is a chiral compound widely used in asymmetric synthesis as a catalyst or ligand. This material plays a crucial role in laboratories where precise control over reaction outcomes is essential. Its unique molecular structure enables it to facilitate complex chemical reactions with high selectivity, particularly in oxidation and reduction processes. It is a key component in the development of chiral compounds with specific stereochemistry, which are vital in pharmaceutical and organic chemistry research.

The compound's ability to provide stereocontrolled outcomes makes it a preferred choice for researchers aiming to produce compounds with defined configurations. Its molecular structure, featuring salicylidene groups attached to a cyclohexane ring, contributes to its stability and effectiveness in various reaction conditions. The presence of multiple chiral centers allows for the synthesis of enantiomerically pure products, which is critical in drug development and bioactive molecule production. This makes it a versatile tool in the hands of chemists and pharmacologists.

In Indonesian laboratories, this compound is commonly used by researchers in the fields of chemistry and pharmacy. It is integral to the development of new compounds, especially in pharmacology and the synthesis of active pharmaceutical ingredients. Its reliability and performance in controlled environments make it a go-to material for advanced chemical research and development projects.

TCI brochures (PDF)

Chiral Ligands 2024-12-13 · p. 2
Asymmetric Synthesis 2026-03-18 · p. 5
Ligands 2025-12-01 · p. 4

Related TCI products

Asymmetric synthesis is a key application where this compound is used to produce enantiomerically pure compounds, essential for pharmaceutical development.
It is widely applied in oxidation and reduction reactions due to its ability to control reaction pathways and enhance selectivity.
In organic chemistry research, it supports the synthesis of complex molecules requiring precise stereochemical control.
It is used in the development of new drugs, where the correct configuration of molecules is critical for biological activity.
The compound is also employed in ligand design for catalytic systems, offering enhanced reactivity and specificity in various chemical transformations.

Brand	TCI
CAS number	135616-36-3
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Catalysts, Chiral Ligands, Chiral Reagents
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid
Storage	Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its stability and effectiveness. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its chemical integrity. Proper labeling of storage containers is essential for safe handling and identification. In laboratory settings, it should be handled with care to avoid contamination and ensure safe disposal. Always follow standard safety protocols when working with chiral compounds to maintain a secure and efficient research environment.

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