CAS 23978-09-8

2,2,2-Cryptand

Description:

2,2,2-Cryptand, also known as 2,2,2-cryptand, is a synthetic organic compound characterized by its unique three-dimensional structure that allows it to encapsulate cations effectively. This cryptand features a rigid framework formed by interconnected nitrogen and carbon atoms, creating a cavity that can selectively bind various metal ions, particularly alkali and alkaline earth metals. The compound exhibits high stability and solubility in polar solvents, making it useful in coordination chemistry and supramolecular chemistry applications. Its ability to form stable complexes with cations is attributed to the presence of multiple donor atoms, which enhance its chelating properties. Additionally, 2,2,2-cryptand has been studied for its potential applications in ion-selective electrodes, extraction processes, and as a ligand in catalysis. The compound's structural features contribute to its selectivity and efficiency in binding, making it a valuable tool in both research and industrial settings. Overall, 2,2,2-cryptand exemplifies the significance of molecular architecture in influencing chemical behavior and interactions.

Formula: C₁₈H₃₆N₂O₆

InChI: InChI=1S/C18H36N2O6/c1-7-21-13-14-24-10-4-20-5-11-25-17-15-22-8-2-19(1)3-9-23-16-18-26-12-6-20/h1-18H2

InChI key: InChIKey=AUFVJZSDSXXFOI-UHFFFAOYSA-N

SMILES: N12CCOCCOCCN(CCOCCOCC1)CCOCCOCC2

Synonyms:

• 2,2,2-Crypt
• 2,2,2-Cryptand
• 2,2,2-Cryptate
• 2,2-Cryptand
• 4,7,13,16,21,24-Hexaoxa-1,10-Diazabiciclo[8.8.8]Hexacosano
• 4,7,13,16,21,24-Hexaoxa-1,10-Diazoniabicyclo[8.8.8]Hexacosane
• 4,7,13,16,21,24-Hexaoxa-1,10-diazabicyclo[8.8.8]hexacosan
• Bicyclo[8.8.8]Hexacosane, 4,7,13,16,21,24-Hexaoxa-1,10-Diaza-
• Crypt-2,2,2
• Cryptand 2.2.2
• Cryptand 222
• Cryptand C 222
• Cryptand C222
• Cryptate 222
• Cryptating agent 222
• Cryptofix 222
• K 222
• Kryptand 222
• Kryptofix 222
• Nsc 264495
• Ws-A 101
• [2,2,2]Crypand

4,7,13,16,21,24-Hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane

CAS: 23978-09-8

Formula: C₁₈H₃₆N₂O₆

Purity: 98%

Color and Shape: Solid, White - Almost white powder

Molecular weight: 376.494

Ref: 10-F239231

Cryptating agent 222

CAS: 23978-09-8

Cryptating agent 222

Formula: C₁₈H₃₆N₂O₆

Purity: ≥98%

Molecular weight: 376.49

Ref: 54-BUP17622

4,7,13,16,21,24-Hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane

CAS: 23978-09-8

4,7,13,16,21,24-Hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane

Formula: C₁₈H₃₆N₂O₆

Purity: 98%

Color and Shape: Solid

Molecular weight: 376.494

Ref: 54-OR74527

4,7,13,16,21,24-Hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane

CAS: 23978-09-8

Formula: C₁₈H₃₆N₂O₆

Purity: 97%

Color and Shape: Solid

Molecular weight: 376.4882

Ref: IN-DA00352Q

4,7,13,16,21,24-Hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane

CAS: 23978-09-8

Formula: C₁₈H₃₆N₂O₆

Purity: >98.0%(GC)(T)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 376.49

Ref: 3B-H0932

4,7,13,16,21,24-Hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane

CAS: 23978-09-8

Color and Shape: Neat

Ref: 86-MM3981.03

2,2,2-Cryptand

CAS: 23978-09-8

Formula: C₁₈H₃₆N₂O₆

Molecular weight: 376.257

Ref: 4Z-E-134052

2,2,2-Crypt

Controlled Product

CAS: 23978-09-8

Applications 2,2,2-Crypt is used in the synthesis of hybrid metal-organic salts. It is also an impurity in the preparation of Fludeoxyglucose (D232570), a D-Glucose (G595000) derivative used in the synthesis of sugar nucleotides and oligosaccharides.
References Marti-R. et al.: New. J. Chem., 38, 1385 (2014);

Formula: C₁₈H₃₆N₂O₆

Color and Shape: Neat

Molecular weight: 376.49

Ref: TR-C827460

Cryptating agent 222

CAS: 23978-09-8

Cryptating agent 222 reduces distannene & creates ligands with metal ions using a potassium mirror.

Formula: C₁₈H₃₆N₂O₆

Purity: 99.91%

Color and Shape: Less Crystals Colourless Crystals

Molecular weight: 376.49

Ref: TM-T20736

4,7,13,16,21,24-Hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane

CAS: 23978-09-8

Hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane (HODHB) is a hexacyclic trisodium salt of a diaza-polycyclic aromatic hydrocarbon that has been used as an imaging agent for cancer tissues. The HODHB ion is formed in the presence of sodium salts and hydrogen fluoride and reacts with nitrogen atoms to form amyloid protein complexes. These complexes are then detected using diagnostic techniques such as preparative high performance liquid chromatography or titration calorimetry. Thermodynamic data was obtained by studying the reaction solution and reaction mechanism. Pharmacokinetic properties were investigated by measuring the stability of complexes in the blood stream over time.

Formula: C₁₈H₃₆N₂O₆

Purity: Min. 97.5%

Molecular weight: 376.49 g/mol

Ref: 3D-FH29194

Fludeoxyglucose Related Compound A (4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane)

CAS: 23978-09-8

Nucleic acids and their salts, whether or not chemically defined; other heterocyclic compounds, nesoi

Formula: C₁₈H₃₆N₂O₆

Color and Shape: Colorless Light Yellow Crystalline Solid

Molecular weight: 376.25734

Ref: 45-1272918