1448722-25-5

Basic information

• Product Name: (2R,3R,4R,5R)-1,3-[(S)-benzylidenedioxy]-5,9-dimethyl-5-vinyldec-8-ene-2,4-diol
• Synonyms: (2R,3R,4R,5R)-1,3-[(S)-benzylidenedioxy]-5,9-dimethyl-5-vinyldec-8-ene-2,4-diol
• CAS NO: 1448722-25-5
• Molecular Weight: 346.467
• Mol File: 1448722-25-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (2R,3R,4R,5R)-1,3-[(S)-benzylidenedioxy]-5,9-dimethyl-5-vinyldec-8-ene-2,4-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R,4R,5R)-1,3-[(S)-benzylidenedioxy]-5,9-dimethyl-5-vinyldec-8-ene-2,4-diol(1448722-25-5)
• EPA Substance Registry System: (2R,3R,4R,5R)-1,3-[(S)-benzylidenedioxy]-5,9-dimethyl-5-vinyldec-8-ene-2,4-diol(1448722-25-5)

Safety Data

• Hazardous Substances Data: 1448722-25-5(Hazardous Substances Data)

Upstream product

• 1174918-98-9 (Z)-2-(3,7-dimethylocta-2,6-dien-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 99274-32-5 2,4-O-benzylidene-D-threose 
• 1057662-85-7 (E)-2-(3,7-dimethylocta-2,6-dien-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 5389-87-7 1-chloro-3,7-dimethylocta-2,6-diene 
• 20536-36-1 neryl chloride 

Relevant articles and documents

Stereoselective construction of all-carbon quaternary stereocenters by allylboration of chiral aldehydes: synthesis of a fragment of (+)-vibsanin A

Stereoselective construction of all-carbon quaternary stereocenters by allylboration of chiral aldehydes is described. Sugar-derived aldehydes were allylated with geranylboronate or nerylboronate to provide γ-adducts possessing quaternary stereocenters wi