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3-Epischelhammericine is a naturally occurring epimer of schelhammericine, which can be found in Phelline comosa. Its structure has been determined through the analysis of spectroscopic data, particularly from nuclear magnetic resonance (NMR) and mass spectra. 3-Epischelhammericine holds potential for various applications due to its unique chemical properties.

24204-36-2

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24204-36-2 Usage

Uses

Used in Pharmaceutical Industry:
3-Epischelhammericine is used as a pharmaceutical compound for its potential therapeutic properties. The compound's unique structure, as revealed by NMR and mass spectra, suggests that it may have applications in the development of new drugs or treatments for various medical conditions.
Used in Chemical Research:
In the field of chemical research, 3-Epischelhammericine serves as a valuable subject for studying the properties and behavior of natural epimers. Its structure and occurrence in Phelline comosa contribute to the understanding of the chemical diversity found in nature, which can lead to the discovery of new compounds with novel applications.
Used in Natural Product Extraction:
3-Epischelhammericine is used as a natural product for extraction and purification from the source plant, Phelline comosa. The compound's isolation can be crucial for further research and development, as well as for potential commercial applications in the pharmaceutical, cosmetic, or other industries that utilize natural products.

References

Langlois, Das, Potier, Compt. Rend., 269C, 639 (1969)

Check Digit Verification of cas no

The CAS Registry Mumber 24204-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,0 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24204-36:
(7*2)+(6*4)+(5*2)+(4*0)+(3*4)+(2*3)+(1*6)=72
72 % 10 = 2
So 24204-36-2 is a valid CAS Registry Number.
InChI:InChI=1/C19H23NO3/c1-21-15-5-4-14-6-8-20-7-2-3-13-9-17-18(23-12-22-17)10-16(13)19(14,20)11-15/h4,9-10,15H,2-3,5-8,11-12H2,1H3/t15-,19-/m0/s1

24204-36-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name C-Homoerythrinan, 1,6-didehydro-3-methoxy-15,16-[methylenebis(oxy)]-, (3.β.)-

1.2 Other means of identification

Product number -
Other names 3-epi-schelhammereicine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:24204-36-2 SDS

24204-36-2Downstream Products

24204-36-2Relevant academic research and scientific papers

ATHROTAXIS ALKALOIDS. PART I. ALKALOIDS OF A. CUPRESSOIDES

Panichanun, Sirichai,Bick, I. Ralph C.

, p. 2677 - 2684 (1984)

Eleven homoerythrina-type alkaloids (1-9, 11, 12) have been isolated from A. cupressoides (Taxodiaceae), of which six (6-9, 11, 12) had not previously been reported.

Total synthesis of homoerythrinan alkaloids, schelhammericine and 3-epischelhammericine

Tsuda, Yoshisuke,Ohshima, Takeshi,Hosoi, Shinzo,Kaneuchi, Satomi,Kiuchi, Fumiyuki,Toda, Jun,Sano, Takehiro

, p. 500 - 508 (2007/10/03)

Total syntheses of two homoerythrinan alkaloids, schelhammericine and 3-epischelhammericine, are described. Photocycloaddition of a dioxopyrrolobenzazepine to 1-methoxy-3-trimethylsilyloxybutadiene afforded, in a regio- and stereo-specific manner, the cyc

Total synthesis of the homoerythrinan alkaloids, schelhammericine and 3-epischelhammericine

Tsuda,Hosoi,Ohshima,et al.

, p. 3574 - 3577 (2007/10/02)

This stereo-coantrolled total synthesis of the title alkaloids, both in racemic form, is the first synthesis of the naturally occurring homoerythrinan alkaloids.

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