EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

muricatacin

Supplier Sponsors

CAS Number: 134698-86-5Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J549.805H
XlogP3-AA:5.80 (est)
Molecular Weight:284.43964000
Formula:C17 H32 O3
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
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Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Soluble in:
 water, 7.495 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
Muricatacin 95%
 
Safety Information:
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
natural substances and extractives
Recommendation for muricatacin usage levels up to:
 not for fragrance use.
 
Recommendation for muricatacin flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :3035657
National Institute of Allergy and Infectious Diseases:Data
(5R)-5-[(1R)-1-hydroxytridecyl]oxolan-2-one
Chemidplus:0134698865
 
References:
 (5R)-5-[(1R)-1-hydroxytridecyl]oxolan-2-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):3035657
Pubchem (cas):134698-86-5
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
CHEMBL:View
HMDB (The Human Metabolome Database):HMDB38685
FooDB:FDB018089
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
EFSA Update of results on the monitoring of furan levels in food:Read Report
EFSA Previous report: Results on the monitoring of furan levels in food:Read Report
EFSA Report of the CONTAM Panel on provisional findings on furan in food:Read Report
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 annona muricata seed
Search Trop Picture
 
Synonyms:
2(3H)-furanone, dihydro-5-(1-hydroxytridecyl)-, (R-(R*,R*))-
(5R)-5-[(1R)-1-hydroxytridecyl]oxolan-2-one
 

Articles:

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.
 
Notes:
None found
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