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Catalogue Number
BN-O1859
Analysis Method
Specification
98%(HPLC)
Storage
2-8°C
Molecular Weight
328.31
Appearance
Botanical Source
Structure Type
Category
SMILES
CC1CC(C2(C13CC(C(C24COC4=O)(C)O)OC(=O)C3O)O)O
Synonyms
IUPAC Name
(1S,2R,4R,5R,6S,7R,8R,11R)-4,5,7,11-tetrahydroxy-2,7-dimethylspiro[9-oxatricyclo[6.3.1.01,5]dodecane-6,3'-oxetane]-2',10-dione
Applications
Density
1.149g/cm3
Solubility
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Flash Point
106.7ºC
Boiling Point
251.2ºC at 760 mmHg
Melting Point
227-228ºC
InChl
InChl Key
GEVWHIDSUOMVRI-QWNPAUMXSA-N
WGK Germany
RID/ADR
HS Code Reference
Personal Projective Equipment
Correct Usage
For Reference Standard and R&D, Not for Human Use Directly.
Meta Tag
provides coniferyl ferulate(CAS#:5230-87-5) 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.
30525614
Since the elucidation of the structure of anisatin in the late 1960s, sesquiterpene lactones from various Illicium species of plants have captivated synthetic chemists worldwide, resulting in a large body of synthetic work. In particular, Illicium sesquiterpenes containing the seco-prezizaane carbon framework have seen immense interest in recent years owing to desirable structural and medicinal attributes. This synopsis will focus on recently developed synthetic strategies to access these compact, highly oxidized terpenoids.
Contemporary Synthetic Strategies toward seco-Prezizaane Sesquiterpenes from Illicium Species
Matthew L Condakes 1, Luiz F T Novaes 1, Thomas J Maimone 1
2018 Dec 21;
27966918
Illicium sesquiterpenes have been the subject of numerous synthetic efforts due to their ornate and highly oxidized structures as well as significant biological activities. Herein we report the first chemical synthesis of (+)-pseudoanisatin from the abundant feedstock chemical cedrol (∼$50 USD/kg) in 12 steps using extensive site-selective C(sp3)-H bond functionalization. Significantly, this work represents a novel oxidative strategic template for future approaches to these natural products and their analogs.
Oxidative Entry into the Illicium Sesquiterpenes: Enantiospecific Synthesis of (+)-Pseudoanisatin
Kevin Hung 1, Matthew L Condakes 1, Takahiro Morikawa 1, Thomas J Maimone 1
2016 Dec 28
26891462
Covering: 1860-2016A mechanistic link may exist between convulsant plant substances typified by picrotoxinin, and ‘neurotrophic’ sesquiterpenes like jiadifenolide. Picrotoxinin elicits convulsion by anion blockade of the Cys-loop family of neurotransmitter-gated ion channels. These same receptors mediate neuronal development and neurite outgrowth prior to synapse formation. Due to its structural homology with picrotoxin and anisatin, it is possible that jiadifenolide enhances NGF-stimulated neurite outgrowth by modulation of the Cys-loop family of receptors.
Neurite outgrowth enhancement by jiadifenolide: possible targets
R A Shenvi 1
2016 Apr