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The chemical compound "4,8-dimethyldecahydro-6H-3,5a-methano-8,13a-propanocyclohepta[h][1,3]oxazolo[3,2-b]isoquinolin-5(2H,13H)-one" is a complex organic molecule with a unique structure. It belongs to the class of compounds known as cyclohepta[h][1,3]oxazoloisoquinolines, which are heterocyclic compounds containing both oxygen and nitrogen atoms in their rings. This specific compound features a decahydro (10-carbon) backbone with a 3,5a-methano bridge, connecting the cyclohepta ring to the isoquinoline system. The molecule also includes two methyl groups at the 4 and 8 positions, which contribute to its overall structure and properties. 4,8-dimethyldecahydro-6H-3,5a-methano-8,13a-propanocyclohepta[h][1,3]oxazolo[3,2-b]isoquinolin-5(2H,13H)-one is characterized by its intricate ring system and the presence of a propano bridge, which distinguishes it from simpler isoquinoline derivatives.

467-93-6

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467-93-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 467-93-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 467-93:
(5*4)+(4*6)+(3*7)+(2*9)+(1*3)=86
86 % 10 = 6
So 467-93-6 is a valid CAS Registry Number.

467-93-6SDS

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 11a-homo-14-nor-isoatisinan-15-one

1.2 Other means of identification

Product number -
Other names Isocuauchichicin

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:467-93-6 SDS

467-93-6Downstream Products

467-93-6Relevant academic research and scientific papers

Construction of "normal"- and "iso-type" oxazolidine rings in C20-diterpenoid alkaloids: Oxidative cyclization with potassium ferricyanide

Pelletier, S.William,Ateya, Abdel-Monem M.,Mody, Naresh V.,Desai, Haridutt K.,Schramm, Lee C.

, p. 3647 - 3650 (2007/10/02)

An efficient and simple method using alkaline ferricyanide for converting the NCH2CH2OH group-containing alkaloid derivatives into their "normal"- and "iso-type"-oxazolidine ring-containing alkaloids has been developed. This is the first one-step oxidation method which affords both types of oxazolidine rings simultaneously.

FORMATION OF THE OXAZOLIDINE RING IN C20-DITERPENOID ALKALOIDS BY OXIDATIVE CYCLIZATION WITH SILVER OXIDE

Pelletier, S. William,Ateya, Abdel-Monem M.,Mody, Naresh V.,Schramm, Lee C.

, p. 1155 - 1157 (2007/10/02)

Treatment of the N-CH2-CH2OH group containing alkaloids with silver oxide in alcohol affords the "iso-type" oxazolidine ring-containing alkaloids in yield 72 to 90percent via oxidative cyclization.This method affords higher yields than earlier reported methods for this type transformation.

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