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(3S,5S)-1-benzyl-5-hydroxymethylpyrrolidin-3-ol is a pyrrolidine derivative chemical compound with the molecular formula C13H17NO2. It features a benzyl group attached to the nitrogen atom and a hydroxymethyl group attached to the 5th carbon atom. (3S,5S)-1-benzyl-5-hydroxymethylpyrrolidin-3-ol holds potential pharmaceutical applications due to its structural resemblance to natural compounds and its pharmacological properties.

635299-92-2

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635299-92-2 Usage

Uses

Used in Pharmaceutical Applications:
(3S,5S)-1-benzyl-5-hydroxymethylpyrrolidin-3-ol is used as a pharmaceutical compound for its potential therapeutic effects. Its structural similarity to natural compounds and pharmacological properties make it a promising candidate for the development of new drugs and treatments.
Used in Drug Design and Development:
In the field of drug design and development, (3S,5S)-1-benzyl-5-hydroxymethylpyrrolidin-3-ol is used as a molecular template for creating new drugs. Its unique structure allows researchers to explore its interactions with various biological targets, potentially leading to the discovery of novel therapeutic agents.
Used in Chemical Research:
(3S,5S)-1-benzyl-5-hydroxymethylpyrrolidin-3-ol is also utilized in chemical research as a starting material or intermediate for the synthesis of more complex molecules. Its unique functional groups and stereochemistry make it a valuable tool for studying reaction mechanisms and developing new synthetic methods.
Used in Analytical Chemistry:
(3S,5S)-1-benzyl-5-hydroxymethylpyrrolidin-3-ol can be employed in analytical chemistry as a reference material or standard for the development and validation of analytical methods. Its distinct chemical properties can be used to calibrate instruments and ensure the accuracy of measurements in various chemical analyses.
Used in Material Science:
(3S,5S)-1-benzyl-5-hydroxymethylpyrrolidin-3-ol may also find applications in material science, particularly in the development of novel materials with specific properties. Its unique structure could be exploited to create new polymers, coatings, or other materials with tailored characteristics for various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 635299-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,5,2,9 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 635299-92:
(8*6)+(7*3)+(6*5)+(5*2)+(4*9)+(3*9)+(2*9)+(1*2)=192
192 % 10 = 2
So 635299-92-2 is a valid CAS Registry Number.

635299-92-2Relevant academic research and scientific papers

1-(DIHYDRONAPHTHALENYL)PYRIDONES AS MELANIN-CONCENTRATING HORMONE RECEPTOR 1 ANTAGONISTS

-

, (2013/10/22)

Provided are 1-(dihydronaphthalenyl)pyridones which are antagonists at the melanin-concentrating hormone receptor 1 (MCHR1), pharmaceutical compositions containing them, processes for their preparation, and their use in therapy for the treatment of obesity and diabetes.

Enantiospecific synthesis and receptor binding of novel dopamine receptor ligands employing natural 4-hydroxyproline as a practical and flexible building block

Heindl, Cornelia,Huebner, Harald,Gmeiner, Peter

, p. 3153 - 3172 (2007/10/03)

Starting from natural 4-hydroxyproline, an ex-chiral pool approach is described giving access to 2-aminoalkylpyrrolidine derivatives that were used as chiral building blocks for the synthesis of bioactive 2-methoxybenzamide derivatives. The 4-hydroxy substituent can be displaced employing organocuprates as useful carbanion equivalents. Dopamine and serotonin binding studies involving the subtypes D1, D2long, D2short, D3 and D4 as well as 5-HT1A and 5-HT2, respectively, provided interesting insights into stereoselective structure activity relationships. The (2S,4R)-2-aminomethylpyrrolidine derivative ent-66 and the (2R,4S)-2- aminoethylpyrrolidine derivative 68 showed remarkable affinity and preference for the dopamine D3 and D4 receptor subtypes, respectively, both being putatively associated to the symptoms of schizophrenia.

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