pluviatolide

2(3H)-furanone, 4-(1,3-benzodioxol-5-ylmethyl)dihydro-3-[(4-hydroxy-3-methoxyphenyl)methyl]-, (3R,4R)-

CAS: 28115-68-6 C20 H20 O6 MW: 356.37460000

Identification

Namepluviatolide
IUPAC(3R,4R)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one
CAS Number28115-68-6
FDA UNIISearch
Molecular FormulaC20 H20 O6
Molecular Weight356.37460000
Nikkaji NumberJ17.298G

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 569.50 °C. @ 760.00 mm Hg (est)
Flash Point 402.00 °F. TCC ( 205.40 °C. ) (est)
logP (o/w) 2.590 (est)
Soluble in water, 12.73 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for pluviatolide usage levels up tonot for fragrance use.
Recommendation for pluviatolide flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

found in nature

Synonyms

(3R,4R)-4- benzo[1,3]dioxol-5-ylmethyl-3-(4-hydroxy-3-methoxy-benzyl)-dihydro-furan-2-one (3R-trans)-4-(1,3- benzodioxol-5-yl methyl)dihydro-3-((4-hydroxy-3-methoxyphenyl)methyl)-2(3H)-furanone (3R,4R)-4-(1,3- benzodioxol-5-ylmethyl)-3-(4-hydroxy-3-methoxybenzyl)dihydro-2(3H)-furanone (3R,4R)-4-(1,3- benzodioxol-5-ylmethyl)-3-(4-hydroxy-3-methoxybenzyl)dihydrofuran-2(3H)-one (3R,4R)-4-(1,3- benzodioxol-5-ylmethyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 2(3H)- furanone, 4-(1,3-benzodioxol-5-ylmethyl)dihydro-3-((4-hydroxy-3-methoxyphenyl)methyl)-, (3R-trans)- 2(3H)- furanone, 4-(1,3-benzodioxol-5-ylmethyl)dihydro-3-[(4-hydroxy-3-methoxyphenyl)methyl]-, (3R,4R)- PubMed: Chemical constituents from Mongolian herb Syringa pinnatifolia var. alashanensis. PubMed: Next generation sequencing in predicting gene function in podophyllotoxin biosynthesis. PubMed: Chemical constituents of Aristolochia constricta: antispasmodic effects of its constituents in guinea-pig ileum and isolation of a diterpeno-lignan hybrid. PubMed: Biosynthesis of yatein in Anthriscus sylvestris. PubMed: Antibiotic activity and absolute configuation of 8S-heptadeca-2(Z),9(Z)-diene-4,6-diyne-1,8-diol from Bupleurum salicifolium. PubMed: [The chemical constituents of Torreyajackii (II)]. PubMed: [The chemical proof of the absolute configurations of di-o-methylhydroxy-thujaplicatin methyl ether, pluviatolide and 2-(3'',4''-dimethoxybenzyl)-3(3', 4'-methylenedioxybenzyl) butyrolactone (author's transl)].