1422278-34-9

Basic information

• Product Name: (1R,2R,3R,4R)-2-methyl-2-(4-methylpent-3-en-1-yl)-3-vinylcyclohexane-1,4-diol
• CAS NO: 1422278-34-9
• Molecular Weight: 238.37
• Mol File: 1422278-34-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1R,2R,3R,4R)-2-methyl-2-(4-methylpent-3-en-1-yl)-3-vinylcyclohexane-1,4-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R,3R,4R)-2-methyl-2-(4-methylpent-3-en-1-yl)-3-vinylcyclohexane-1,4-diol(1422278-34-9)
• EPA Substance Registry System: (1R,2R,3R,4R)-2-methyl-2-(4-methylpent-3-en-1-yl)-3-vinylcyclohexane-1,4-diol(1422278-34-9)

Safety Data

• Hazardous Substances Data: 1422278-34-9(Hazardous Substances Data)

Upstream product

• 638-37-9 butanedial 
• 21214-62-0 (Z)-4,8-dimethyl-nona-1,3,7-triene 

Downstream Products

• 1422278-36-1 C₂₉H₃₄O₄ 
• 1422278-38-3 C₂₉H₃₂Br₂O₄ 

Relevant articles and documents

A catalytic enantioselective tandem allylation strategy for rapid terpene construction: Application to the synthesis of pumilaside aglycon

Catalytic enantioselective 1,2-diboration of 1,3-dienes followed by cascade allylborations with dicarbonyls provides rapid entry into carbocyclic reaction products. The stereochemical course of this reaction was studied along with its application in the synthesis of pumilaside aglycon.