• TCI B3970 1197922-04-5 (11bS)-2,6-Bis[bis[3,5-bis(trifluoromethyl)phenyl]hydroxymethyl]-3,5-dihydrospiro[4H-dinaphth[2,1-c:1',2'-e]azepine-4,4'-morpholinium] Bromide
  • 1197922-04-5 (11bS)-2,6-Bis[bis[3,5-bis(trifluoromethyl)phenyl]hydroxymethyl]-3,5-dihydrospiro[4H-dinaphth[2,1-c:1',2'-e]azepine-4,4'-morpholinium] Bromide - AMI Scientific
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TCI

CAS 1197922-04-5

(11bS)-2,6-Bis[bis[3,5-bis(trifluoromethyl)phenyl]hydroxymethyl]-3,5-dihydrospiro[4H-dinaphth[2,1-c:1',2'-e]azepine-4,4'-morpholinium] Bromide TCI B3970

(11bS)-2,6-Bis[bis[3,5-bis(trifluoromethyl)phenyl]hydroxymethyl]-3,5-dihydrospiro[4H-dinaphth[2,1-c:1',2'-e]azepine-4,4'-morpholinium] Bromide TCI B3970

Chemical Identity

CAS No.
1197922-04-5
PubChem
CID 44597114·SID 160870901
Formula
C60H36BrF24NO3
Molecular weight
1354.8 g/mol
Purity
>97.0%(HPLC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
[16'-[bis[3,5-bis(trifluoromethyl)phenyl]-hydroxymethyl]spiro[1,4-oxazinan-4-ium-4,13'-13-azoniapentacyclo[13.8.0.02,11.03,8.018,23]tricosa-1(15),2(11),3,5,7,9,16,18,20,22-decaene]-10'-yl]-bis[3,5-bis(trifluoromethyl)phenyl]methanol bromide
SMILES
C1COCC[N+]12CC3=C(C4=CC=CC=C4C=C3C(C5=CC(=CC(=C5)C(F)(F)F)C(F)(F)F)(C6=CC(=CC(=C6)C(F)(F)F)C(F)(F)F)O)C7=C(C2)C(=CC8=CC=CC=C87)C(C9=CC(=CC(=C9)C(F)(F)F)C(F)(F)F)(C1=CC(=CC(=C1)C(F)(F)F)C(F)(F)F)O.[Br-]
InChIKey
UVHZWWMJSAGSJH-UHFFFAOYSA-M
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This complex compound is a specialized reagent used in asymmetric synthesis, particularly in reactions requiring chiral catalysts. It plays a critical role in enantioselective reactions, enabling the production of specific asymmetric structures with high efficiency. Its molecular structure allows for precise interactions with substrates, enhancing the selectivity and yield of desired products. As a chiral catalyst, it is essential for researchers aiming to control stereochemistry in organic reactions. Its unique properties make it a valuable tool in the development of new compounds and pharmaceuticals.

The compound’s complex molecular architecture provides exceptional reactivity and specificity, making it a preferred choice for advanced synthetic applications. It is known for its stability under controlled conditions, which ensures consistent performance in laboratory settings. Its ability to direct reactions toward specific products is unmatched, offering researchers greater control over reaction outcomes. This makes it particularly useful in complex molecular synthesis where precision is paramount. The compound’s effectiveness in promoting enantioselectivity has led to its widespread use in both academic and industrial research.

In Indonesian laboratories, this material is commonly used in organic chemistry research, especially in projects focused on drug development and molecular synthesis. Its application extends to pharmaceutical and biochemical studies, where the ability to produce chiral compounds with high selectivity is crucial. Researchers in Indonesia rely on this compound for its reliability and performance in challenging synthetic conditions, making it an essential component of modern chemical research.

Advantages (TCI brochure)

  • Enables enantioselective conjugate addition of 3-substituted oxindoles under neutral conditions
  • Works without base additives in water-rich solvent

TCI brochures (PDF)

Related TCI products

  • Asymmetric synthesis projects benefit from this compound’s ability to direct reactions toward specific enantiomers, enhancing product selectivity and yield.
  • Pharmaceutical research utilizes it for the synthesis of chiral compounds, which are critical in drug development and bioavailability studies.
  • Organic chemistry experiments rely on its unique catalytic properties to achieve complex molecular transformations with high stereocontrol.
  • Biochemical studies use it to explore enzyme-like catalytic behavior in synthetic systems, mimicking natural processes.
  • Advanced research in molecular design leverages its structural complexity to create novel compounds with tailored properties for various applications.

From the TCI brochure

  • Conjugate addition of 3-substituted oxindoles to Michael acceptors

Brand TCI
CAS number 1197922-04-5
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Catalysts, Chiral Ligands, Chiral Reagents
Pack sizes —
Physical form —
Storage Requires protection from moisture and air exposure

Data from the TCI brochure

PelarutH2O/toluene (reaksi adisi konjugasi)

Source: TCI brochure R5111 (2025-06-12)

This compound should be stored in a cool, dry environment away from moisture and air to maintain its chemical stability. It is recommended to use airtight containers made of materials that do not react with the compound, such as glass or high-density polyethylene. Laboratory personnel should handle the material with care, using appropriate personal protective equipment to avoid direct contact. Due to its sensitivity, it should be stored in a controlled environment to prevent degradation. Regular monitoring of storage conditions ensures the compound remains effective for its intended applications. Proper labeling and safe handling practices are essential to maintain laboratory safety and product integrity.

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