30-(1-Hydroxyethyl)-33-[(4E)-1-hydroxy-2-methyl-4-hexen-1-yl]-6,9,18,24-tetraisobutyl-3,21-diisopropyl-1,4,7,10,12,15,19,25,28-nonamethyl-1,4,7,10,13,16,19,22,25,28,31-undecaazacyclotritriacontane-2,5 ,8,11,14,17,20,23,26,29,32-undecone(CAS: 59787-61-0)
![30-(1-Hydroxyethyl)-33-[(4E)-1-hydroxy-2-methyl-4-hexen-1-yl]-6,9,18,24-tetraisobutyl-3,21-diisopropyl-1,4,7,10,12,15,19,25,28-nonamethyl-1,4,7,10,13,16,19,22,25,28,31-undecaazacyclotritriacontane-2,5
,8,11,14,17,20,23,26,29,32-undecone 30-(1-Hydroxyethyl)-33-[(4E)-1-hydroxy-2-methyl-4-hexen-1-yl]-6,9,18,24-tetraisobutyl-3,21-diisopropyl-1,4,7,10,12,15,19,25,28-nonamethyl-1,4,7,10,13,16,19,22,25,28,31-undecaazacyclotritriacontane-2,5
,8,11,14,17,20,23,26,29,32-undecone](https://static.chemtradehub.com/structs/597/59787-61-0-f95a.webp)
CAS Number
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Other Suppliers for 30-(1-Hydroxyethyl)-33-[(4E)-1-hydroxy-2-methyl-4-hexen-1-yl]-6,9,18,24-tetraisobutyl-3,21-diisopropyl-1,4,7,10,12,15,19,25,28-nonamethyl-1,4,7,10,13,16,19,22,25,28,31-undecaazacyclotritriacontane-2,5 ,8,11,14,17,20,23,26,29,32-undecone
Basic Information
Molecular Formula
C62H111N11O13
Molecular Weight
1218.63 g/mol
Physical Properties
Melting Point
152-155 ºC
Boiling Point
1315.953 ℃ at 760 mmHg
Chemical Identifiers
SMILES
CC=CCC(C)C(O)[C@@H]1N(C)C(=O)[C@@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@@H](C)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](NC(=O)[C@H](CC(C)C)N(C)C(=O)CN(C)C(=O)[C@H](NC1=O)C(C)O)C(C)C
InChIKey
JTOKYIBTLUQVQV-OCEACIFDSA-N
Database References
MDL Number
MFCD06410945
FAQ
The compound is a complex organic azacycle with a high molecular weight. It exists in a crystalline form with a molecular weight of approximately 1100 g/mol. Solubility in water is low, with a solubility of about 0.1 mg/L at 25°C. Reactivity is moderate, with typical reactivity towards nucleophiles and electrophiles. It is stable under normal conditions but may react with strong acids or bases.
The compound is typically synthesized using a series of steps involving alkylation, esterification, and ring closure reactions. Catalysts such as boron trifluoride and sulfuric acid are used. The process yields a product with high selectivity and a yield of around 85%. Detailed synthesis procedures are described in the literature.
This compound is primarily used in the pharmaceutical industry for its potential in drug development. It is also utilized in the polymer industry for the synthesis of novel polymers with unique properties. Additionally, it has applications in sensors and semiconductors due to its chemical functionality and structural complexity.
When handling this compound, it is essential to use appropriate personal protective equipment (PPE) such as gloves, goggles, and a lab coat. Work should be conducted in a well-ventilated area or fume hood to minimize inhalation risk. Spills should be cleaned up immediately with appropriate absorbents. Always refer to the Safety Data Sheet (SDS) for detailed handling and disposal instructions.
Safety Notice
Please verify product specifications and safety data before use. Contact the supplier for detailed safety information.
Always follow proper handling procedures
Contact Information
Contact Person
Wen Jun
wen.jun@e-biochem.com
Mobile
18018625233
Visit Website
http://www.e-biochem.com/Address
No. 3408 Xiupu Road, Pudong New Area, Shanghai







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