445380-28-9

Basic information

• Product Name: 4,6-bis[(2-methoxyethoxy)methyloxy]-2-[(1'E,6'R,10'S)-6',10'-dihydroxyundec-1'-en-1'-yl]benzoic acid
• Synonyms: 4,6-bis[(2-methoxyethoxy)methyloxy]-2-[(1'E,6'R,10'S)-6',10'-dihydroxyundec-1'-en-1'-yl]benzoic acid
• CAS NO: 445380-28-9
• Molecular Weight: 514.613
• Mol File: 445380-28-9.mol

Chemical Properties

• CAS DataBase Reference: 4,6-bis[(2-methoxyethoxy)methyloxy]-2-[(1'E,6'R,10'S)-6',10'-dihydroxyundec-1'-en-1'-yl]benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4,6-bis[(2-methoxyethoxy)methyloxy]-2-[(1'E,6'R,10'S)-6',10'-dihydroxyundec-1'-en-1'-yl]benzoic acid(445380-28-9)
• EPA Substance Registry System: 4,6-bis[(2-methoxyethoxy)methyloxy]-2-[(1'E,6'R,10'S)-6',10'-dihydroxyundec-1'-en-1'-yl]benzoic acid(445380-28-9)

Safety Data

• Hazardous Substances Data: 445380-28-9(Hazardous Substances Data)

Upstream product

• 445380-26-7 methyl 4,6-bis[(2-methoxyethoxy)methyloxy]-2-[(1'E,6'R,10'S)-6',10'-bis(tert-butyldimethylsilyloxy)undec-1'-en-1'-yl]benzoate 
• 311805-54-6 (5R,9S)-5,9-bis(tert-butyldimethylsilyloxy)decan-1-ol 
• 311805-75-1 (5S,9S)-5,9-bis(tert-butyldimethylsilyloxy)decanal 
• 311805-71-7 diethyl (6-benzyloxy-2-oxo-1-hexyl)phosphonate 
• 445380-24-5 (1'E,4R,5S)-4-(7'-benzyloxy-3'-oxohept-1'-en-1'-yl)-2,2,5-trimethyl-1,3-dioxolane 
• 311805-52-4 (1'E,2RS,4S,5S)-4-(7'-benzyloxy-3'-oxohept-1'-en-1'-yl)-5-methyl-1,3-dioxa-2-thiolane 2-oxide 
• 445380-25-6 (6E,8S,9S)-1-benzyloxy-8,9-dihydroxydec-6-en-5-one 
• 445380-27-8 methyl 4,6-bis[(2-methoxyethoxy)methyloxy]-2-[(1'E,6'R,10'S)-6',10'-dihydroxyundec-1'-en-1'-yl]benzoate 

Downstream Products

• 36455-72-8 α-zearalenol 
• 40790-12-3 (E)-(7R,11R)-2,4,11-Trihydroxy-7-methyl-7,8,9,10,11,12,13,14-octahydro-6-oxa-benzocyclotetradecen-5-one 

Relevant articles and documents

The use of π-allyltricarbonyliron lactone complexes in the synthesis of the resorcylic macrolides α- and β-zearalenol

A highly stereoselective synthesis of the natural products α- and β-zearalenol 1 and 2 has been achieved using π-allyltricarbonyliron lactone complexes to control the 1,5-stereochemical relationship of the oxygen functionalities found in these resorcylic macrolides.

The use of π-allyltricarbonyliron lactone complexes in the synthesis of the resorcylic macrolides α- and β-zearalenol

A highly stereoselective synthesis of α- and β-zearalenol 1 and 2 is accomplished utilising π-allyltricarbonyliron lactone complexes 5 and 6 to establish the 1,5-stereochemical relationship of oxygen functionalities present in the natural products. The Royal Society of Chemistry 2000.