Catalogue Number
BN-O1656
Analysis Method
HPLC,NMR,MS
Specification
98%(HPLC)
Storage
-20℃
Molecular Weight
204.2
Appearance
Yellow powder
Botanical Source
This product is isolated and purified from the herbs of Cerbera manghas L.
Structure Type
Iridoids
Category
Standards;Natural Pytochemical;API
SMILES
COC(=O)C1=COC=C2C1=CC=C2C=O
Synonyms
Cyclopenta[c]pyran-4-carboxylic acid, 7-formyl-, methyl ester/Methyl 7-formylcyclopenta[c]pyran-4-carboxylate
IUPAC Name
methyl 7-formylcyclopenta[c]pyran-4-carboxylate
Density
1.3±0.1 g/cm3
Solubility
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Flash Point
198.8±27.4 °C
Boiling Point
433.4±40.0 °C at 760 mmHg
Melting Point
InChl
InChI=1S/C11H8O4/c1-14-11(13)10-6-15-5-9-7(4-12)2-3-8(9)10/h2-6H,1H3
InChl Key
PNHQFFOWCUDBPX-UHFFFAOYSA-N
WGK Germany
RID/ADR
HS Code Reference
2932990000
Personal Projective Equipment
Correct Usage
For Reference Standard and R&D, Not for Human Use Directly.
Meta Tag
provides coniferyl ferulate(CAS#:65597-42-4) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate
No Technical Documents Available For This Product.
11706272
The molecule of the title compound, methyl 1-formyl-6-oxa-6H-indene-4-carboxylate, C(11)H(8)O(4), is planar. There are weak C–H…O intramolecular interactions and an intermolecular hydrogen bond in the structure, and these influence the crystal packing.
Atomic charges of cerbinal.
Laphookhieo S1, Karalai C, Chantrapromma S, Fun HK, Usman A, Rat-a-Pa Y, Chantrapromma K.
2001 Nov
31452369
Owing to the changing needs of agriculture, the exploration of new pest control agents remains as critical as ever. The analogues 3a-3v of the natural product cerbinal were synthesized from genipin by an efficient and practical method under additive-free conditions. The antiviral and insecticidal effects of cerbinal and these cyclopenta[c]pyridines (3a-3v) were evaluated systematically. Most of the synthesized compounds exhibited higher anti-TMV activities than the lead compound cerbinal. Compound 3s (2-(4-methoxyphenyl)) had the most promising inhibitory activities against TMV (inactivation effect 49.0 ± 0.8%, curative effect 41.2 ± 4.3%, and protection effect 51.5 ± 2.7% at 500 μg/mL). Among the synthesized compounds, only 3v (2-(2-chloro-4-(trifluoromethoxy)phenyl)) reached the activity level of cerbinal against Plutella xylostella. This suggested that the cyclopenta[c]pyridines obtained by modifications of cerbinal at position 2 are very significant for the anti-TMV activity, and yet were exceptionally less active for the insecticidal activities.
anti-TMV activity; cerbinal; cyclopenta[]pyridines; insecticidal activities; natural product; synthesis
Natural Product Cerbinal and Its Analogues Cyclopenta[c]pyridines: Synthesis and Discovery as Novel Pest Control Agents.
2019 Sep 18
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