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27510-33-4

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27510-33-4 Usage

Description

O-Methylpallidine【Corydalis】 is an alkaloid that has been recently isolated from Rhigiocarya racemifera, a plant species where it is predominantly found in the roots. O-Methylpallidine【Corydalis】 is known for its potential medicinal properties and is being studied for its various applications in the pharmaceutical and related industries.

Uses

Used in Pharmaceutical Industry:
O-Methylpallidine【Corydalis】 is used as a pharmaceutical compound for its potential therapeutic effects. The alkaloid is being investigated for its possible applications in the treatment of various health conditions due to its unique chemical properties and interactions with biological systems.
Used in Traditional Medicine:
In traditional medicine, O-Methylpallidine【Corydalis】 is used as a natural remedy for various ailments. Its presence in the roots of Rhigiocarya racemifera has led to its inclusion in herbal formulations and treatments, leveraging its potential medicinal benefits.
Used in Research and Development:
O-Methylpallidine【Corydalis】 is also used in the research and development of new drugs and therapies. Its isolation from a natural source provides a valuable starting point for scientists to study its mechanisms of action, potential synergies with other compounds, and its overall safety and efficacy.
Used in Drug Delivery Systems:
Similar to gallotannin, O-Methylpallidine【Corydalis】 could potentially be employed in drug delivery systems to enhance its bioavailability and therapeutic outcomes. By incorporating this alkaloid into novel drug delivery platforms, researchers may be able to improve its delivery to target tissues and cells, thereby increasing its effectiveness in treating specific health conditions.

References

Tackie et al., Phytochem., 13,2884 (1974)

Check Digit Verification of cas no

The CAS Registry Mumber 27510-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,5,1 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 27510-33:
(7*2)+(6*7)+(5*5)+(4*1)+(3*0)+(2*3)+(1*3)=94
94 % 10 = 4
So 27510-33-4 is a valid CAS Registry Number.

27510-33-4SDS

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 O-Methylpallidine

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:27510-33-4 SDS

27510-33-4Downstream Products

27510-33-4Relevant articles and documents

Synthesis of optically active aporphine and morphinandienone alkaloids via p-quinol esters

Hara,Komoriya,Miyashita,Hoshino

, p. 1683 - 1692 (2007/10/02)

Lead tetraacetate oxidation of N-trifluoroacetylnorcodamine (5) in (S)-(+)-2-phenylpropionic acid gave a diastereomeric mixture of two p-quinol acylates, which were easily separated to enantiomerically pure 6a and 6b. Treatment of the chiral quinol acylates (6a) and (6b) with trifluoroacetic acid in CH2Cl2 at room temperature afforded (1R)-(-)-6-trifluoroacetylwilsonirine (7a) and (1S)-(+)-(7b), respectively. Saponification of 7a and 7b gave rise to (-)-wilsonirine (8a) and its enantiomer (8b), respectively. Similarly, (-)-nordomesticine (12a) and (+)-(12b) were synthesized in enantiomerically pure form from 10a and 10b. On the other hand, acid treatment of 6a and 6b in CH3CN at lower temperature (-30°C) llowed by N-deprotection gave the corresponding normorphinandienones (15a and 15b) as major products, which were transformed to enantiomerically pure (-)-16a and (+)-sebiferine (16b). In a similar sequence of reactions, (+)-amurine (19a) and its enantiomer (19b) were synthesized.

Alkaloids of Ocotea acutangula

Vecchietti, Vittorio,Casagrande, Cesare,Ferrari, Giorgio,Danieli, Bruno,Palmisano, Giovanni

, p. 578 - 581 (2007/10/02)

The leaves of Ocotea acutangula (Mez) contain, in addition to the known (S)-(-)-pallidine (5) and its new derivative (S)-(-)-O-methylpallidine (6), the new 8,14-dihydromorphinandienone alkaloids (S)-(-)-pallidinine (7) and (S)-(-)-O-methylpallidinine (8) which possess a B/C trans-junction.

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