85909-35-9 Usage
Uses
Used in Pharmaceutical Industry:
(S)-3-[[(acetylamino)methyl]thio]-2-aminopropionamide is used as a building block for the development of new drugs due to its unique structural features and potential biological activity. The presence of thioether and amide groups, along with the specific stereochemistry, may contribute to its interaction with biological targets, making it a promising candidate for the creation of novel therapeutic agents.
Used in Chemical Research:
In the field of chemical research, (S)-3-[[(acetylamino)methyl]thio]-2-aminopropionamide serves as a model compound for studying the effects of stereochemistry on molecular properties and reactivity. Its unique structure allows researchers to explore the influence of different functional groups and stereochemistry on the compound's behavior, which can be applied to the design of more effective and selective drugs.
Used in Material Science:
(S)-3-[[(acetylamino)methyl]thio]-2-aminopropionamide may also find applications in material science, particularly in the development of novel materials with specific properties. (S)-3-[[(acetylamino)methyl]thio]-2-aminopropionamide's unique structure and functional groups could be utilized to create materials with tailored characteristics, such as improved stability, reactivity, or selectivity in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 85909-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,0 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85909-35:
(7*8)+(6*5)+(5*9)+(4*0)+(3*9)+(2*3)+(1*5)=169
169 % 10 = 9
So 85909-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H13N3O2S/c1-4(10)9-3-12-2-5(7)6(8)11/h5H,2-3,7H2,1H3,(H2,8,11)(H,9,10)
85909-35-9Relevant academic research and scientific papers
Hydrophobic parameters ? of amino-acid side chains from the partitioning of N-acetyl-amino-acid amides
Fauchere, Jean-Luc,Pliska, Vladimir
, p. 369 - 376 (2007/10/02)
A hydrophobic parameter for the side chain of each of the twenty naturally occuring amino-acids was estimated quantitatively by partitioning of their N-acetyl-amino-acid amides (CH3CO-NH-CH(R)-CONH2, R=variable side chain) in octanol/water.Suitable forms of the derivatives were synthesized chemically where necessary.The new series affords reliable distribution coefficients especially for polar amino-acids.A set of Hansch side chain parameters ? obtained for the twenty common amino-acids, for half-cystine as well as for the extremly lipophilic amino-acids carboranylalanine and adamantylalanine.It is found that these hydrophobicity indices, obtained at neutral pH, are tightly correlated with the degree of solvent exposure of the side chain in globular proteins and it is proposed that they be used in future biophysical and pharmacological studies.
