116073-68-8

Basic information

• Product Name: 1,9,17-Trioxa-5,13,21-triazacyclotetracosane, 13-[(4-methylphenyl)sulfonyl]-
• CAS NO: 116073-68-8
• Molecular Formula: C25H45N3O5S
• Molecular Weight: 499.715
• Mol File: 116073-68-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,9,17-Trioxa-5,13,21-triazacyclotetracosane, 13-[(4-methylphenyl)sulfonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,9,17-Trioxa-5,13,21-triazacyclotetracosane, 13-[(4-methylphenyl)sulfonyl]-(116073-68-8)
• EPA Substance Registry System: 1,9,17-Trioxa-5,13,21-triazacyclotetracosane, 13-[(4-methylphenyl)sulfonyl]-(116073-68-8)

Safety Data

• Hazardous Substances Data: 116073-68-8(Hazardous Substances Data)

Upstream product

• 116073-67-7 21-tosyl-1,9,17-trioxa-5,13,21-triazacyclotetracosane-6,12-dione 
• 1656-48-0 2-cyanoethyl ether 
• 111-94-4 3,3'-Iminodipropionitrile 
• 5961-83-1 3-(2-carboxyethoxy)propionic acid 
• 44995-78-0 3,3'oxybispropionic acid dichloride 
• 2619-16-1 N,N-bis[(2-cyanoethyl)]-4-methylbenzenesulfonamide 
• 98-59-9 p-toluenesulfonyl chloride 
• 116073-65-5 N-tosyl-3,3'-iminobis-1-(2-cyanoethoxy)propane 
• 116073-66-6 N-tosyl-3,3'-iminobis-1-(3-aminopropoxy)propane 
• 56187-12-3 N-tosyl-bis(3-hydroxypropyl)amine 
• 5446-58-2 3,3'-iminodipropanoic acid tosylamide 

Downstream Products

• 116073-79-1 C₆₆H₉₄N₆O₁₄S₂ 
• 116073-81-5 C₄₅H₅₇N₃O₁₂ 
• 116073-82-6 5,13,21-tris(4-carboxybenzoyl)-1,9,17-trioxa-5,13,21-triazacyclotetracosane 
• 116073-83-7 C₄₂H₄₈Cl₃N₃O₉ 
• 116073-77-9 C₄₁H₅₃N₃O₁₁S 
• 116073-78-0 C₄₁H₅₁Cl₂N₃O₉S 

Relevant articles and documents

MACROCYCLIC AND MACROPOLYCYCLIC COMPOUNDS BASED UPON 1,3-DISUBSTITUTED PROPANE UNITS

Synthetic routes to the macrocyclic polyamine derivatives (1) and (3) are described, together with an investigation of the complexing properties of the triamines (1d) and (3d) with primary alkylammonium cations.Macrotricyclic and macrotetracyclic compounds may be obtained from the macrocycle (1) by a stepwise procedure whereas macrocycle (3b) can be converted into a macrotricyclic derivative in a one step alkylation procedure.The alkylation of the tetrahydropyrimidone (18) with α,α'-dibromo-m-xylene gives the calix arene analogue (19) which adopts the 'cone' (21a) and '1,3-alternate' (21b) conformations.The macrocyclic hexa-amine (23) may be synthesized by a simple alkylation procedure whereas the octa-amine (27) required a systematic stepwise synthesis.The hexa-amine salt (23)*6 HBr shows selectivity in forming inclusion complexes with the dicarboxylate anions (1-)O2C(CH2)nCO2(1-).