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(3R,4aS,8aS)-2-(tert-butoxycarbonyl)decahydroisoquinoline-3-carboxylic acid is a bicyclic organic compound with a molecular formula of C17H29NO4. It is a derivative of decahydroisoquinoline, which has a structure resembling a condensed form of piperidine and cyclohexane rings. (3R,4aS,8aS)-2-(tert-butoxycarbonyl)decahydroisoquinoline-3-carboxylic acid features a tert-butoxycarbonyl group, a protective group used in organic synthesis, and a carboxylic acid group, indicating its acidic nature. Its unique functional groups and structure may offer potential applications in organic synthesis, medicinal chemistry, and drug development.

252008-88-1

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252008-88-1 Usage

Uses

Used in Organic Synthesis:
(3R,4aS,8aS)-2-(tert-butoxycarbonyl)decahydroisoquinoline-3-carboxylic acid is used as an intermediate in organic synthesis for [application reason]. The presence of the tert-butoxycarbonyl group allows for the protection of reactive functionalities, facilitating complex synthetic sequences.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (3R,4aS,8aS)-2-(tert-butoxycarbonyl)decahydroisoquinoline-3-carboxylic acid is used as a building block for the development of novel pharmaceuticals due to its unique structure and functional groups, which can be further modified to create bioactive molecules.
Used in Drug Development:
(3R,4aS,8aS)-2-(tert-butoxycarbonyl)decahydroisoquinoline-3-carboxylic acid is utilized as a potential candidate in drug development, particularly for targeting specific biological pathways or receptors. Its carboxylic acid group may facilitate interactions with biological targets, and its overall structure could be optimized for improved potency and selectivity.
Used in Pharmaceutical Industry:
(3R,4aS,8aS)-2-(tert-butoxycarbonyl)decahydroisoquinoline-3-carboxylic acid is used as a key component in the development of new drugs for various therapeutic areas within the pharmaceutical industry, leveraging its structural and functional features to create innovative medicines.
Additional testing and research would be required to fully understand the potential uses and properties of (3R,4aS,8aS)-2-(tert-butoxycarbonyl)decahydroisoquinoline-3-carboxylic acid, as well as to optimize its application in different fields.

Check Digit Verification of cas no

The CAS Registry Mumber 252008-88-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,0,0 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 252008-88:
(8*2)+(7*5)+(6*2)+(5*0)+(4*0)+(3*8)+(2*8)+(1*8)=111
111 % 10 = 1
So 252008-88-1 is a valid CAS Registry Number.

252008-88-1Upstream product

252008-88-1Downstream Products

252008-88-1Relevant academic research and scientific papers

Substituted piperidines as melanocortin-4 receptor agonists

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Page column 56, (2010/02/05)

Certain novel substituted piperidine compounds are agonists of the human melanocortin receptor(s) and, in particular, are selective agonists of the human melanocortin-4 receptor (MC-4R). They are therefore useful for the treatment, control, or prevention of diseases and disorders responsive to the activation of MC-4R, such as obesity, diabetes, sexual dysfunction, including erectile dysfunction and female sexual dysfunction. Also provided are methods of treating sexual dysfunction with a compound that is a selective agonist of MC-4R over any other human melanocortin receptor.

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