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4846-19-9

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4846-19-9 Usage

Description

(R)-Nornuciferine, an alkaloid derived from Hottuynia cordata, is a bioactive compound with significant pharmacological properties. It is characterized by its potential anti-inflammatory activity and is a promising candidate for various therapeutic applications.

Uses

Used in Pharmaceutical Industry:
(R)-Nornuciferine is used as a therapeutic agent for its anti-inflammatory properties, which can be beneficial in the treatment of various inflammatory conditions and diseases. Its natural origin and potential to modulate immune responses make it a valuable addition to the pharmaceutical sector.
Used in Nutraceutical Applications:
In the nutraceutical industry, (R)-Nornuciferine can be utilized as an ingredient in dietary supplements and functional foods due to its anti-inflammatory and potential health-promoting benefits. Its incorporation into these products may contribute to overall wellness and support a healthy immune system.
Used in Cosmetics and Personal Care:
(R)-Nornuciferine's anti-inflammatory properties can also be harnessed in the cosmetics and personal care industry. It may be used as an active ingredient in skincare products, targeting inflammation-related skin conditions such as acne, rosacea, or eczema, and promoting a healthier skin appearance.
Used in Research and Development:
As a bioactive compound with potential therapeutic applications, (R)-Nornuciferine is valuable in research and development for the discovery of new drugs and therapies. Its study can lead to a better understanding of its mechanisms of action and the development of novel treatments for various health conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 4846-19-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,4 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4846-19:
(6*4)+(5*8)+(4*4)+(3*6)+(2*1)+(1*9)=109
109 % 10 = 9
So 4846-19-9 is a valid CAS Registry Number.

4846-19-9SDS

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 N-Nornuciferine

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:4846-19-9 SDS

4846-19-9Relevant articles and documents

Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry

Casagrande, Gleison A.,Deflon, Victor M.,Martins, Gabriel R.,Oliveira-Silva, Diogo,Perecim, Givago P.,Pinto, Leandro M. C.,Raminelli, Cristiano

, (2020/08/13)

Total syntheses of (S)- and (R)-nuciferine were accomplished through approach involving diastereoselective reaction between a chiral dihydroisoquinoline enamide and 2-(trimethylsilyl)phenyl trifluoromethanesulfonate promoted by CsF, affording a separable mixture of diastereoisomers, which provided (S)- and (R)-nuciferine via simple and efficient transformations.

Aporphine alkaloid synthesis and diversification via direct arylation

Lafrance, Marc,Blaquiere, Nicole,Fagnou, Keith

, p. 811 - 825 (2008/02/12)

Palladium-catalyzed direct arylation of aryl chlorides, bromides and iodides has been applied to the preparation of new aporphine analogues including C2-substituted aporphines by reaction with benzodioxole, pyridine N-oxide and pyrazine N-oxide. Successful application of direct arylation in these diversification reactions highlights its utility not only in convergent, but also in divergent synthesis. We also describe enantioselective syntheses of (R)-nornuciferine and (R)-nuciferine employing a catalytic asymmetric transfer hydrogenation in high yield and excellent enantiomeric excess. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.

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