78808-86-3

Basic information

• Product Name: 3,5,5-Trimethyl-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,3,4-trimethyl-phenyl)-octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-cyclohex-3-enone
• Synonyms: 3,5,5-Trimethyl-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,3,4-trimethyl-phenyl)-octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-cyclohex-3-enone
• CAS NO: 78808-86-3
• Molecular Weight: 546.836
• Mol File: 78808-86-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,5,5-Trimethyl-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,3,4-trimethyl-phenyl)-octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-cyclohex-3-enone(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5,5-Trimethyl-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,3,4-trimethyl-phenyl)-octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-cyclohex-3-enone(78808-86-3)
• EPA Substance Registry System: 3,5,5-Trimethyl-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,3,4-trimethyl-phenyl)-octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-cyclohex-3-enone(78808-86-3)

Safety Data

• Hazardous Substances Data: 78808-86-3(Hazardous Substances Data)

Upstream product

• 78854-48-5 Acetic acid 3,5,5-trimethyl-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,3,4-trimethyl-phenyl)-octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-cyclohex-3-enyl ester 
• 64354-70-7 Triphenyl-(2,3,4-trimethylbenzyl)-phosphoniumbromid 
• 25494-52-4 O-acetyl-β-citraurin 
• 78854-49-6 3,5,5-Trimethyl-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,3,4-trimethyl-phenyl)-octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-cyclohex-3-enol 

Downstream Products

• 55511-20-1 tedanin 
• 78808-85-2 Acetic acid 3,5,5-trimethyl-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,3,4-trimethyl-phenyl)-octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-cyclohexa-1,3-dienyl ester 

Relevant articles and documents

PARTIAL SYNTHESIS OF AROMATIC CAROTENOIDS, TEDANIN, AGELAXANTHIN A, TETHYATENE, AND RENIERATENE

Aromatic carotenoids, tedanin, agelaxanthin A, and tethyatene were synthesized from O-acetyl-β-citraurin derived from natural zeaxanthin, and tethyatene was further transformed into renieratene as the first example of aromatization of an alicyclic ring in