77798-78-8

Basic information

• Product Name: 2,5-Bis(13-bromtridecanoylamino)-3,6-bis<12-(tetrahydro-2-pyranyloxy)dodecyl>hydrochinon-dimethylether
• CAS NO: 77798-78-8
• Molecular Weight: 1255.53
• Mol File: 77798-78-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,5-Bis(13-bromtridecanoylamino)-3,6-bis<12-(tetrahydro-2-pyranyloxy)dodecyl>hydrochinon-dimethylether(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Bis(13-bromtridecanoylamino)-3,6-bis<12-(tetrahydro-2-pyranyloxy)dodecyl>hydrochinon-dimethylether(77798-78-8)
• EPA Substance Registry System: 2,5-Bis(13-bromtridecanoylamino)-3,6-bis<12-(tetrahydro-2-pyranyloxy)dodecyl>hydrochinon-dimethylether(77798-78-8)

Safety Data

• Hazardous Substances Data: 77798-78-8(Hazardous Substances Data)

Upstream product

• 77798-75-5 2,5-Dinitro-3,6-bis<12-(tetrahydro-2-pyranyloxy)dodecyl>hydrochinon-dimethylether 
• 77798-73-3 2,5-Bis<11-(methoxycarbonyl)undecyl>-3,6-dinitrohydrochinon-dimethylether 
• 77798-72-2 12-[4-(11-Carboxy-undecyl)-2,5-dihydroxy-3,6-dinitro-phenyl]-dodecanoic acid 
• 77798-64-2 2,5-Bis(11-carboxyundecyl)-3,6-dinitro-1,4-benzochinon 
• 77798-61-9 2,5-Bis(11-carboxyundecyl)hydrochinon-diacetat 
• 77798-74-4 2,5-Bis(12-hydroxydodecyl)-3,6-dinitrohydrochinon-dimethylether 
• 77798-57-3 2,5-Bis(11-methoxycarbonyl-1-undecenyl)hydrochinon-dimethylether 
• 77798-58-4 2,5-Bis<11-(methoxycarbonyl)undecyl>hydrochinon-dimethylether 
• 343859-17-6 12-[4-(11-Carboxy-undecyl)-2,5-dihydroxy-phenyl]-dodecanoic acid 
• 1108-58-3 <10-(Methoxycarbonyl)decyl>triphenylphosphoniumiodid 
• 15462-16-5 13-bromotridecanoic acid 
• 61657-98-5 13-Bromtridecanoylchlorid 
• 343862-95-3 2,5-Dimethoxy-3,6-bis-[12-(tetrahydro-pyran-2-yloxy)-dodecyl]-benzene-1,4-diamine 

Relevant articles and documents

Synthese von zweifach ueberbrueckten 2,5-Diamino-1,4-dialkyl-3,6-dimethoxybenzol-Derivaten als -Praerotaxane

Starting with 2,5-dimethoxyterephthaldialdehyde (1) and the triphenylphosphorane 2 the double bridged 2,5-diaminohydroquinone derivative 20 is synthesised in a multistep reaction sequence.Via the dibromide 21 as intermediate, the -prerotaxane 22 is obt