15356-41-9 Usage
Uses
Used in Pharmaceutical Industry:
(2R,3R,4S,5S)-5,6,6-tris(ethylsulfanyl)hexane-1,2,3,4-tetrol (non-preferred name) is used as a potential pharmaceutical compound for its unique stereochemistry and functional groups. The presence of multiple hydroxyl and ethylsulfanyl groups may allow for interactions with biological targets or serve as a building block for the development of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, (2R,3R,4S,5S)-5,6,6-tris(ethylsulfanyl)hexane-1,2,3,4-tetrol (non-preferred name) can be utilized as a versatile intermediate or reagent. Its specific configuration and functional groups may enable the synthesis of complex organic molecules or the modification of existing compounds to enhance their properties or create new functionalities.
Used as a Reagent in Chemical Reactions:
(2R,3R,4S,5S)-5,6,6-tris(ethylsulfanyl)hexane-1,2,3,4-tetrol (non-preferred name) may also serve as a reagent in various chemical reactions, such as esterification, condensation, or substitution reactions. Its unique structure and functional groups can facilitate specific chemical transformations or improve the efficiency and selectivity of certain processes.
Check Digit Verification of cas no
The CAS Registry Mumber 15356-41-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,5 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15356-41:
(7*1)+(6*5)+(5*3)+(4*5)+(3*6)+(2*4)+(1*1)=99
99 % 10 = 9
So 15356-41-9 is a valid CAS Registry Number.
15356-41-9Relevant academic research and scientific papers
Characterization and interconversions of 2-S-ethyl-2-thio-D-mannose diethyl dithioacetal and the facile epimerization of 2-thio-D-mannopyranose derivatives
Horton, Derek,Norris, Peter,Berrang, Bertold
, p. 53 - 71 (2007/10/03)
3,4,5,6-Tetra-O-benzoyl-D-glucose diethyl dithioacetal (2) reacts with ethanethiol under acidic conditions to afford 3,4,5,6-tetra-O-benzoyl-2-S-ethyl-2-thio-D-mannose (3), the stereochemistry at C-2 of which has been assigned by chemical conversions on i
