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Anisatin

$3,600

  • Brand : BIOFRON

  • Catalogue Number : BN-O1859

  • Specification : 98%(HPLC)

  • CAS number : 5230-87-5

  • Formula : C15H20O8

  • Molecular Weight : 328.31

  • PUBCHEM ID : 115121

  • Volume : 20mg

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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.

PMID

30525614

Abstract

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.

Title

Contemporary Synthetic Strategies toward seco-Prezizaane Sesquiterpenes from Illicium Species

Author

Matthew L Condakes 1, Luiz F T Novaes 1, Thomas J Maimone 1

Publish date

2018 Dec 21;

PMID

27966918

Abstract

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.

Title

Oxidative Entry into the Illicium Sesquiterpenes: Enantiospecific Synthesis of (+)-Pseudoanisatin

Author

Kevin Hung 1, Matthew L Condakes 1, Takahiro Morikawa 1, Thomas J Maimone 1

Publish date

2016 Dec 28

PMID

26891462

Abstract

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.

Title

Neurite outgrowth enhancement by jiadifenolide: possible targets

Author

R A Shenvi 1

Publish date

2016 Apr