99877-53-9

Basic information

• Product Name: (1R,2S,3R)-3-[(4E)-6-hydroxy-5-methyl-1-methylidenehex-4-en-1-yl]-1,2-dimethylcyclopentanol
• CAS NO: 99877-53-9
• Molecular Formula: C₁₅H₂₆O₂
• Molecular Weight: 238.3657
• Mol File: 99877-53-9.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 350.7°C at 760 mmHg
• Flash Point: 156.7°C
• Density: 0.98g/cm³
• Vapor Pressure: 2.58E-06mmHg at 25°C
• Refractive Index: 1.503
• CAS DataBase Reference: (1R,2S,3R)-3-[(4E)-6-hydroxy-5-methyl-1-methylidenehex-4-en-1-yl]-1,2-dimethylcyclopentanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2S,3R)-3-[(4E)-6-hydroxy-5-methyl-1-methylidenehex-4-en-1-yl]-1,2-dimethylcyclopentanol(99877-53-9)
• EPA Substance Registry System: (1R,2S,3R)-3-[(4E)-6-hydroxy-5-methyl-1-methylidenehex-4-en-1-yl]-1,2-dimethylcyclopentanol(99877-53-9)

Safety Data

• Hazardous Substances Data: 99877-53-9(Hazardous Substances Data)

Upstream product

• 152092-93-8 (1R,2S,3R)-1-Methyl-3-(5-methyl-1-methylene-hex-4-enyl)-2-trimethylsilanylmethyl-cyclopentanol 

Relevant articles and documents

The effect of tether substituents on the selectivity of Pd catalyzed enyne cyclizations. A total synthesis of chokol C

In the context of the palladium catalyzed cycloisomerization of enynes, two of the most important tether substituents, the carbonyl group because of its general synthetic versatility and the ketal because of its prospect to induce absolute stereochemistry by employing the ketal from a chiral diol, are probed within the context of a synthesis of chokol C, an antifungal compound produced by Phleum pratense when infected by a pathogenic fungus Epichloe typhina.