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9-METHOXY-1,2-METHYLENEDIOXY-7-OXAPORPHINE is an oxoaporphine alkaloid that has been isolated from the eHCl3 extract of the trunk bark of Michelia lanuginosa Wall. Its structure has been confirmed through ultraviolet, infrared, NMR, and mass spectra analysis. Despite attempts to reduce the alkaloid using NaBH4 or catalytic hydrogenation with PtO2, these efforts have been unsuccessful due to the rapid oxidation of the reduction product in solution.

23740-25-2

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23740-25-2 Usage

Uses

Used in Pharmaceutical Industry:
9-METHOXY-1,2-METHYLENEDIOXY-7-OXAPORPHINE is used as a pharmaceutical compound for its potential therapeutic applications. The alkaloid's unique structure and properties make it a candidate for further research and development in the field of medicine.
Used in Chemical Research:
In the field of chemical research, 9-METHOXY-1,2-METHYLENEDIOXY-7-OXAPORPHINE serves as a subject of study for understanding its chemical properties, reactivity, and potential interactions with other compounds. This knowledge can be applied to develop new synthetic methods or explore its use in various chemical processes.
Used in Natural Product Extraction:
9-METHOXY-1,2-METHYLENEDIOXY-7-OXAPORPHINE is used as a natural product extracted from the trunk bark of Michelia lanuginosa Wall. This extraction process can be optimized and scaled up for commercial purposes, providing a source of the alkaloid for various applications in the pharmaceutical, chemical, and other industries.
Used in Analytical Chemistry:
The alkaloid's unique spectral characteristics make it useful in analytical chemistry for the development of new methods and techniques for the identification and quantification of similar compounds. This can lead to advancements in the field of analytical chemistry and improve the detection and analysis of complex mixtures containing oxoaporphine alkaloids.

References

Talapatra, Patra, Talapatra., Chem. Ind., 31, 1056 (1969)

Check Digit Verification of cas no

The CAS Registry Mumber 23740-25-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,4 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23740-25:
(7*2)+(6*3)+(5*7)+(4*4)+(3*0)+(2*2)+(1*5)=92
92 % 10 = 2
So 23740-25-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H11NO4/c1-21-10-2-3-11-12(7-10)17(20)16-14-9(4-5-19-16)6-13-18(15(11)14)23-8-22-13/h2-7H,8H2,1H3

23740-25-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name LANUGINOSINE

1.2 Other means of identification

Product number -
Other names 10-Methoxy-8H-benzo[g]-1,3-benzodioxolo[6,5,4-de]quinolin-8-one

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:23740-25-2 SDS

23740-25-2Downstream Products

23740-25-2Relevant articles and documents

SYNTHESIS OF NOVEL 7,7'-BIS-6a,7-DEHYDRONORAPORPHINES

Jossang, Akino,Leboeuf, Michel,Cave, Andre

, p. 2191 - 2198 (2007/10/02)

New dimers, (+/-)-bisdehydroanonaine 5a, (+/-)-bisdehydroxylopine 5c, (+/-)-bisdehydronornantenine 5d and (+/-)-7-dehydroxylopinyl-7'-dehydronornantenine 8, and the previously described (+/-)-urabaine 5b, were prepared from dehydroxylopine 3c and known dehydronoraporphines 3a, 3b, and 3d via dimerization at the β-carbon of cyclic secondary enamines.

OXOANOLOBINE, A NEW OXOAPORPHINE ALKALOID FROM GUATTERIA MELOSMA

Phoebe, Charles H.,Shiff, Paul L.,Knapp, Joseph E.,Slatkin, David J.

, p. 1977 - 1978 (2007/10/02)

Oxoanolobine (1), a new alkaloid from an alcoholic extract of Guatteria melosma Diels (Anonaceae), was characterized as 1,2-methylenedioxy-9-hydroxyoxoaporphine (10-hydroxy-8H-benzo-1,3-benzodioxoloquinolin-8-one) by physicochemical data and conversion to lanuginosine (2).

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