96645-97-5

Basic information

• Product Name: 2(R)-exo-hydroxy-1,4-cineole
• CAS NO: 96645-97-5
• Molecular Weight: 170.252
• Mol File: 96645-97-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2(R)-exo-hydroxy-1,4-cineole(CAS DataBase Reference)
• NIST Chemistry Reference: 2(R)-exo-hydroxy-1,4-cineole(96645-97-5)
• EPA Substance Registry System: 2(R)-exo-hydroxy-1,4-cineole(96645-97-5)

Safety Data

• Hazardous Substances Data: 96645-97-5(Hazardous Substances Data)

Upstream product

• 470-67-7 1,4-cineole 
• 22555-57-3 2-exo-hydroxy-1-methyl-4-(1-methylethyl)-7-oxabicyclo[2.2.1]heptane 
• 111613-34-4 2-Oxo-(1R,4S)-cineole 
• 2438-10-0 (+)-terpinen-4-ol 
• 20126-76-5 (-)-terpinen-4-ol 

Downstream Products

• 117306-80-6 2(S)-endo-hydroxy-1(S),4(R)-cineole (R)-(-)-O-acetylmandelate 
• 117306-76-0 2(R)-exo-hydroxy-1(S),4(R)-cineole (S)-(+)-O-acetylmandelate 
• 117306-77-1 2(R)-endo-hydroxy-1(R),4(S)-cineole (S)-(+)-O-acetylmandelate 

Relevant articles and documents

Stereochemistry of Microbiological Hydroxylations of 1,4-Cineole

The stereochemistries of microbial hydroxylations of 1-methyl-4-(1-methylethyl)-7-oxabicycloheptane (1,4-cineole)were examined with Bacillus cereus and Streptomyces griseus as biocatalysts.Growing cultures of these bacteria introduce hydroxyl group

PREPARATION OF BIOLOGICALLY ACTIVE SUBSTANCES AND ANIMAL AND MICROBIAL METABOLITES FROM MENTHOLS, CINEOLES AND KAURANES

Six monoterpenoids, l-menthol, l-menthyl acetate, iso-menthol, neo-menthol, 1,4-cineole and 1,8-cineole and one diterpene hydrocarbon, ent-kaurene were oxidized by meta-chloroperbenzoic acid or dry ozone to give various hydroxylated products and their structures elucidated by NMR spectroscopy.Some hydroxylated menthols showed plant growth inhibitory and strong mosquito repellent activity.Among the hydroxylated cineoles, microbial and animal metabolites of cineoles were included.From ent-kauranes, a plant growth inhibitory diterpene alcohol, (-)-16α-hydroxy kaurane was obtained along with 16α-kauran-13α-ol.