muricatacin

CAS: 134698-86-5 C17 H32 O3 MW: 284.43964000

Identification

Namemuricatacin
CAS Number134698-86-5
FDA UNIISearch
Molecular FormulaC17 H32 O3
Molecular Weight284.43964000
Nikkaji NumberJ549.805H

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Soluble in water, 7.495 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 muricatacin usage levels up tonot for fragrance use.
Recommendation for muricatacin flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

annona muricata seed

Synonyms

2(3H)- furanone, dihydro-5-(1-hydroxytridecyl)-, (R-(R*,R*))- (5R)-5-[(1R)-1- hydroxytridecyl]oxolan-2-one PubMed: Concise stereoselective total synthesis of (+)-muricatacin and (+)-epi-muricatacin. PubMed: A chiron approach to the total synthesis of cytotoxic (+)-muricatacin and (+)-5-epi-muricatacin from D-ribose. PubMed: Design, synthesis and antiproliferative activity of two new heteroannelated (-)-muricatacin mimics. PubMed: Synthesis of annonaceous acetogenins from muricatacin. PubMed: An efficient oxidative lactonization of 1,4-diols catalyzed by Cp*Ru(PN) complexes. PubMed: De novo asymmetric syntheses of muricatacin and its analogues via dihydroxylation of dienoates. PubMed: Synthesis and antitumour activity of new muricatacin and goniofufurone analogues. PubMed: Novel cytotoxic monotetrahydrofuranic Annonaceous acetogenins from Annona montana. PubMed: Concise total synthesis of (-)-muricatacin by tandem ring-closing/cross metathesis. PubMed: Total synthesis of (+)-muconin. PubMed: Synthesis of (--)-Muricatacin via alpha- and alpha'-C-H bond functionalization of tetrahydrofuran. PubMed: Unexpected stereochemistry in the lithium salt catalyzed ring expansion of nonracemic oxaspiropentanes. formal syntheses of (-)-(4R,5R)-muricatacin and the pheromone (R)-japonilure. PubMed: A novel constituent from Rollinia mucosa, rollicosin, and a new approach to develop annonaceous acetogenins as potential antitumor agents. PubMed: Syntheses and cytotoxicities of four stereoisomers of muricatacin from D-glucose. PubMed: Parallel, Stereoselective Syntheses of both Enantiomers of Muricatacin and Their Sulfur and Nitrogen Relatives Using the Silyloxy Diene-Based Methodology. PubMed: Synthesis of (-)-muricatacin.