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

cochliophilin A

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CAS Number: 110204-45-0Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J489.635A
XlogP3-AA:3.20 (est)
Molecular Weight:282.25170000
Formula:C16 H10 O5
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
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
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, 7.755 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.
Cochliophilin A
 
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 cochliophilin A usage levels up to:
 not for fragrance use.
 
Recommendation for cochliophilin A 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 :927642
National Institute of Allergy and Infectious Diseases:Data
9-hydroxy-6-phenyl-[1,3]dioxolo[4,5-g]chromen-8-one
 
References:
 9-hydroxy-6-phenyl-[1,3]dioxolo[4,5-g]chromen-8-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):927642
Pubchem (cas):110204-45-0
 
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):HMDB34445
FooDB:FDB012852
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 spinacia oleracea
Search Trop Picture
 
Synonyms:
9-hydroxy-6-phenyl-[1,3]dioxolo[4,5-g]chromen-8-one
 

Articles:

PubMed:Novel Flavones from the Root of Phytolacca acinosa Roxb.
PubMed:Ultrastructure of Aphanomyces cochlioides zoospores and changes during their developmental transitions triggered by the host-specific flavone cochliophilin A.
PubMed:Variation in chemotactic preferences of Aphanomyces cochlioides zoospores to flavonoids.
PubMed:Secondary metabolites from nonhost plants affect the motility and viability of phytopathogenic Aphanomyces cochlioides zoospores.
PubMed:Dynamic rearrangement of F-actin organization triggered by host-specific plant signal is linked to morphogenesis of Aphanomyces cochlioides zoospores.
PubMed:Phenolic constituents of Celosia cristata L. susceptible to spinach root rot pathogen Aphanomyces cochlioides.
PubMed:Quantification of the particle method for chemotactic bioassay using Peronosporomycete zoospores.
PubMed:A photoaffinity probe designed for host-specific signal flavonoid receptors in phytopathogenic Peronosporomycete zoospores of Aphanomyces cochlioides.
PubMed:The third naturally occurring attractant toward zoospores of phytopathogenic Aphanomyces cochlioides from the Spinacia oleracea host plant.
 
Notes:
None found
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