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8-acetyl-14-benzoylchasmanine is a complex organic compound derived from chasmanine, a naturally occurring alkaloid found in the Chasmanthe genus of plants. This specific derivative features an acetyl group attached to the 8th carbon atom and a benzoyl group attached to the 14th carbon atom, which significantly alters its chemical properties and potential applications. The compound is known for its potential biological activities, such as anti-inflammatory and antimicrobial effects, and is of interest to researchers in the field of natural product chemistry and drug discovery. Its unique structure and functional groups make it a subject of study for understanding the structure-activity relationships in alkaloid chemistry and for exploring its potential therapeutic uses.

4296-54-2

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4296-54-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4296-54-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,9 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4296-54:
(6*4)+(5*2)+(4*9)+(3*6)+(2*5)+(1*4)=102
102 % 10 = 2
So 4296-54-2 is a valid CAS Registry Number.
InChI:InChI=1/C34H47NO8/c1-7-35-17-32(18-38-3)14-13-24(40-5)34-22-15-21-23(39-4)16-33(43-19(2)36,26(30(34)35)28(41-6)29(32)34)25(22)27(21)42-31(37)20-11-9-8-10-12-20/h8-12,21-30H,7,13-18H2,1-6H3

4296-54-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 13,15-Dideoxyaconitine

1.2 Other means of identification

Product number -
Other names 8-Acetyl-14-benzoylchasmanine

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:4296-54-2 SDS

4296-54-2Downstream Products

4296-54-2Relevant academic research and scientific papers

Studies on Aconitum species. XV. Deoxygenation reaction of aconitine type alkaloids

Mori,Murayama,Bando,Kawahara

, p. 2803 - 2806 (2007/10/02)

Mesaconitine (1) in tetrahydrofuran reacted with sodium hydride, a catalytic amount of imidazole, carbon disulfide and methyl iodide at room temperature to give the di-O-(S-methyl)thiocarbonate (5). The reductive cleavage of 5 with tri-n-butyltin hydride

STRUCTURE OF EZOCHASMANINE, EZOCHASMACONITINE, ANISOEZOCHASMACONITINE AND SYNTHESIS OF VILMORRIANINE A

Takayama, Hiromitsu,Ito, Miyuki,Koga, Miyuki,Sakai, Shin-ichiro,Okamoto, Toshihiko

, p. 403 - 408 (2007/10/02)

The structures of new diterpene alkaloids, ezochasmanine, ezochasmaconitine, and anisoezochasmaconitine, have been established as 3-hydroxychasmanine, 14-acetyl-8-benzoylchasmanine, and 14-acetyl-8-anisoylchasmanine respectively, in correlation with a known alkaloid chasmanine.Vilmorrianine A (8-acetyl-14-anisoylezochasmanine) was synthesized from ezochasmanine via benzoylation, trichloroethoxycarbonylation, acetylation and elimination reaction of trichloroethoxycarbonyl group.

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