coronarin E, 117591-81-8

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CODE156873 CODE156873
Product(s):
117591-81-8 Coronarin E >98%
Coronarin E, a natural diterpenoid found in the rhizomes of Hedychium coronarium,exhibits the activity of antiplasmodial. anti-plasmodial

Name:	3-[(E)-2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]furan
CAS Number:	117591-81-8	3D/inchi
FDA UNII:	Search
Nikkaji Web:	J595.112G
XlogP3-AA:	6.20 (est)
Molecular Weight:	284.44236000
Formula:	C20 H28 O
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, 0.003988 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.

Coronarin E >98%

Odor: characteristic

Use: Coronarin E, a natural diterpenoid found in the rhizomes of Hedychium coronarium,exhibits the activity of antiplasmodial. anti-plasmodial

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 coronarin E usage levels up to:
	not for fragrance use.

Recommendation for coronarin E 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 :9971144

National Institute of Allergy and Infectious Diseases:Data

3-[(E)-2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]furan

References:

	3-[(E)-2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]furan
NIST Chemistry WebBook:	Search Inchi
Pubchem (cid):	9971144
Pubchem (cas):	117591-81-8

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):	Search
VCF-Online:	VCF Volatile Compounds in Food
ChemSpider:	View
Wikipedia:	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

	alpinia smithiae Search Trop Picture
	curcuma mangga Search Trop Picture
	hedychium yunnanense Search Trop Picture
	mertensia maritima Search Trop Picture

Synonyms:

3-{(E)-2-[(1S,4aS,8aS)-5,5,8a-	trimethyl-2-methylenedecahydro-1-naphthalenyl]vinyl}furan
	furan, 3-[(E)-2-[(1S,4aS,8aS)-decahydro-5,5,8a-trimethyl-2-methylene-1-naphthalenyl]ethenyl]-
3-[(E)-2-[(1S,4aS,8aS)-5,5,8a-	trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]furan

Articles:

PubMed:Labdane-type diterpenes from Hedychium gardnerianum with potent cytotoxicity against human small cell lung cancer cells.

PubMed:[Studies on chemical constituents from rhizomes of Hedychium chrysoleucum].

PubMed:Concise syntheses of coronarin A, coronarin E, austrochaparol and pacovatinin A.

PubMed:Synthesis of chinensines A-E.

PubMed:Facile access to optically active labdane-type diterpenes from (+)-manool. Synthesis of (+)-coronarin E, (+)-15,16-epoxy-8(17),13(16),14-labdatriene, and (+)-labda-8(17),13(Z)-diene-15,16-diol.

PubMed:New diterpene from Hedychium villosum.

PubMed:A concise conversion of (-)-sclareol into (+)-coronarin E and (-)-7-epi-coronarin A

Notes:

None found

coronarin E 3-{(E)-2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylenedecahydro-1-naphthalenyl]vinyl}furan

Supplier Sponsors

Articles:

coronarin E
3-{(E)-2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylenedecahydro-1-naphthalenyl]vinyl}furan