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Bebeerine iodide, O-dimethyl, is a chemical compound with the molecular formula C21H24N2O2I. It is derived from the natural alkaloid bebeerine, which is found in the plant Uncaria tomentosa, commonly known as cat's claw. The O-dimethyl derivative of bebeerine iodide is synthesized by adding two methyl groups to the oxygen atom in the original bebeerine molecule. This modification may alter the chemical properties and potential applications of the compound. Bebeerine iodide, O-dimethyl, has been studied for its potential anti-inflammatory, antioxidant, and immunomodulatory effects, although further research is needed to fully understand its therapeutic potential and safety profile.

5096-67-3

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5096-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5096-67-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,9 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5096-67:
(6*5)+(5*0)+(4*9)+(3*6)+(2*6)+(1*7)=103
103 % 10 = 3
So 5096-67-3 is a valid CAS Registry Number.

5096-67-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Bebeerine iodide, O-dimethyl-

1.2 Other means of identification

Product number -
Other names BEBEERINE IODIDE,TRIHYDRATE

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:5096-67-3 SDS

5096-67-3Downstream Products

5096-67-3Relevant academic research and scientific papers

THE BIOSYNTHESIS OF THE ALKALOIDS OF CISSAMPELOS PAREIRA LINN

Bhakuni,Dewan S.,Jain,Sudha,Chaturvedi,Rekha

, p. 3975 - 3982 (2007/10/02)

Tracer experimets show that the bisbenzylisoqunoline alkaloid,(S,R)-hayatidin (10) is stereospecifically biosynthesized in young Cissampelos pareira Linn plants by intermolecular oxidativ coupling of (S)-(5)-and (R)-(3)-N-methylcoclaurines whereas (R,R)-isochondrodendrine (14) and (R,R)-bebeerine (12) are formed in the plants by oxidative dimerization of (R)-N-methyl-coclaurine (3).

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