111008-73-2

Basic information

• Product Name: (E)-3-[2-((Z)-2-{(E)-1-Hydroxy-3-[2-((Z)-2-{(E)-1-hydroxy-3-[2-((Z)-2-hydroxy-vinyl)-furan-3-yloxy]-allyloxy}-vinyl)-furan-3-yloxy]-allyloxy}-vinyl)-furan-3-yloxy]-propenal
• Synonyms: (E)-3-[2-((Z)-2-{(E)-1-Hydroxy-3-[2-((Z)-2-{(E)-1-hydroxy-3-[2-((Z)-2-hydroxy-vinyl)-furan-3-yloxy]-allyloxy}-vinyl)-furan-3-yloxy]-allyloxy}-vinyl)-furan-3-yloxy]-propenal
• CAS NO: 111008-73-2
• Molecular Weight: 540.48
• Mol File: 111008-73-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-3-[2-((Z)-2-{(E)-1-Hydroxy-3-[2-((Z)-2-{(E)-1-hydroxy-3-[2-((Z)-2-hydroxy-vinyl)-furan-3-yloxy]-allyloxy}-vinyl)-furan-3-yloxy]-allyloxy}-vinyl)-furan-3-yloxy]-propenal(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-[2-((Z)-2-{(E)-1-Hydroxy-3-[2-((Z)-2-{(E)-1-hydroxy-3-[2-((Z)-2-hydroxy-vinyl)-furan-3-yloxy]-allyloxy}-vinyl)-furan-3-yloxy]-allyloxy}-vinyl)-furan-3-yloxy]-propenal(111008-73-2)
• EPA Substance Registry System: (E)-3-[2-((Z)-2-{(E)-1-Hydroxy-3-[2-((Z)-2-{(E)-1-hydroxy-3-[2-((Z)-2-hydroxy-vinyl)-furan-3-yloxy]-allyloxy}-vinyl)-furan-3-yloxy]-allyloxy}-vinyl)-furan-3-yloxy]-propenal(111008-73-2)

Safety Data

• Hazardous Substances Data: 111008-73-2(Hazardous Substances Data)

Upstream product

• 6367-37-9 3,3-diethoxypropanal 

Relevant articles and documents

FORMATION AND POLYMERISATION OF MALONALDEHYDE DURING IRRADIATION OF AQUEOUS SOLUTIONS OF D-GLUCOSE AND LACTOSE WITH ULTRASOUND

Irradiation with ultrasound, vigorous stirring, or vibration of aqueous solutions of D-glucose and lactose can induce chemical reactions.Malonaldehyde has been identified as one product, and the influence of pH and gas atmosphere on its formation by irradiation with ultrasound has been investigated.Only traces were present in neutral solutions, but it was major product in alkaline solutions.Malonaldehyde is unstable, especially in neutral and acidic solutions, and gives 1,3,5-benzenetricarbaldehyde by 1,2-addition and 1 by 1,4-addition.There is evidence that cyclic structures also exist, the ring closure being brought about by an additional hemiacetal bond.To some extent also, 1,3,5-benzenetricarbaldehyde is incorporated into the oligomers.