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"5,8,11-trioxa-2,14-diazabicyclo[13.2.2]nonadeca-1(17),15(19)-diene-16,18-dione" is a complex organic compound characterized by its unique molecular structure. It features a bicyclic arrangement with three oxygen atoms (trioxa) and two nitrogen atoms (diazabicyclo), which contribute to its ring system. The compound is further defined by the positions of its carbonyl groups (dione) at the 16th and 18th carbon atoms, and the double bonds in the diene system between the 15th and 19th carbon atoms. This chemical structure endows the compound with specific properties and potential applications in various fields, such as pharmaceuticals or materials science, although the exact uses would depend on its specific physical and chemical characteristics.

7235-41-8

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7235-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7235-41-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,3 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7235-41:
(6*7)+(5*2)+(4*3)+(3*5)+(2*4)+(1*1)=88
88 % 10 = 8
So 7235-41-8 is a valid CAS Registry Number.

7235-41-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,8,11-trioxa-2,14-diazabicyclo[13.2.2]nonadeca-1(18),15-diene-17,19-dione

1.2 Other means of identification

Product number -
Other names -

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:7235-41-8 SDS

7235-41-8Relevant academic research and scientific papers

A total synthesis of (±)-codeine by 1,3-dipolar cycloaddition

Erhard, Thomas,Ehrlich, Gunnar,Metz, Peter

supporting information; experimental part, p. 3892 - 3894 (2011/06/24)

Nitrone cycloaddition on a dearomatized bicyclic phenol enabled the facile construction of the correctly configured phenanthrene skeleton of codeine. Further steps yielded allopseudocodeine in a completely diastereoselective manner and finally (±)-codeine by allylic transposition through the hydrolysis of chlorocodides.

SYNTHESIS OF MORPHINE AND RELATED DERIVATIVES

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Page/Page column 84-85, (2010/12/17)

The present invention relates to methods for the synthesis of galanthamine, morphine, intermediates, salts and derivatives thereof, wherein the starting compound is biphenyl.

Process for converting neopinone to codeinone

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, (2008/06/13)

A process for converting neopinone alkaloid to codeinone alkaloid which involves treating neopinone with a hydrohalic acid in a suitable solvent under anhydrous conditions. It also relates to the compound 8-halodihydrocodeinone hydrohalide.

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