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(-)-[4aS-(4aα,6β,8aR)]-4a,5,9,10,11,12-hexahydro-3-[13CD3]-methoxy-11-methyl-6H-benzofuro[3a,3,2-e,f][2]-benzazepin-3,6-diol hydrobromide is a complex organic compound with a unique molecular structure. It consists of a mixture of carbon, hydrogen, oxygen, and bromine atoms, as well as deuterium at specific positions. (-)-[4aS-(4aα,6β,8aR)]-4a,5,9,10,11,12-hexahydro-3-[13CD3]-methoxy-11-methyl-6H-benzofuro[3a,3,2-e,f][2]-benzazepin-3,6-diol hydrobromide has potential pharmaceutical applications due to its distinct molecular conformation and properties, which could make it suitable for use in medicinal treatments.

2140262-53-7

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2140262-53-7 Usage

Uses

Used in Pharmaceutical Industry:
(-)-[4aS-(4aα,6β,8aR)]-4a,5,9,10,11,12-hexahydro-3-[13CD3]-methoxy-11-methyl-6H-benzofuro[3a,3,2-e,f][2]-benzazepin-3,6-diol hydrobromide is used as a potential pharmaceutical agent for medicinal treatments. Its unique molecular structure and properties make it a promising candidate for further research and testing to fully understand its potential applications and effects in the development of new drugs and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 2140262-53-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,1,4,0,2,6 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2140262-53:
(9*2)+(8*1)+(7*4)+(6*0)+(5*2)+(4*6)+(3*2)+(2*5)+(1*3)=107
107 % 10 = 7
So 2140262-53-7 is a valid CAS Registry Number.

2140262-53-7Upstream product

2140262-53-7Downstream Products

2140262-53-7Relevant academic research and scientific papers

Synthesis of 3H-, 14C-, and stable-isotope-labelled galantamine

Janssen,Thijssen, Jos B. A.,Verluyten, Willy L. M.

, p. 841 - 855 (2002)

Reminyl is a newly approved drug, used in the treatment of mild to moderate Alzheimer disease. The active compound, galantamine, was initially isolated from the bulbs of certain Narcissus species, but is at the moment also produced synthetically. In the process leading to the final approval, the synthesis of tritium-, carbon-14- and stable-isotope-labelled galantamine for pharmacokinetic studies was required. Racemic (±)-1-bromonarwedine, a compound available as intermediate from the commercial synthesis, was transformed to racemic 1-bromo-galantamine. Catalytic bromo-tritium exchange, followed by HPLC purification and resolution afforded tritium-labelled galantamine. The [14C]-label was introduced on the nitrogen as well as on the oxygen-methyl position. This was achieved by N- and O-demethylation of galantamine and reaction of the thoroughly purified intermediate with [14C]-methyl iodide. Stable-isotope-labelled galantamine was obtained likewise by 13CD3OD-methylation of O-demethylated galantamine under Mitsunobu conditions. Copyright

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