308103-61-9 Usage
Description
(S)-(-)-1,2-Epithiododecane, a chiral molecule with a unique sulfur-containing structure, is known for its two enantiomers that are mirror images of each other. (S)-(-)-1 2-EPITHIODODECANE is often utilized as a synthetic building block in organic chemistry due to its distinctive structure, which is also beneficial for studying chiral recognition and enzymatic reactions. Furthermore, it has garnered attention in the field of biology for its antimicrobial properties, indicating potential applications in the development of new antibiotics or antifungal agents.
Uses
Used in Organic Chemistry:
(S)-(-)-1,2-Epithiododecane is used as a synthetic building block for its unique structure, which aids in the development of various organic compounds.
Used in Chiral Recognition Studies:
(S)-(-)-1 2-EPITHIODODECANE is used as a research tool for studying chiral recognition due to its chiral molecule nature with two enantiomers.
Used in Enzymatic Reaction Research:
(S)-(-)-1,2-Epithiododecane is used in the investigation of enzymatic reactions, taking advantage of its unique sulfur-containing structure.
Used in Biology and Pharmaceutical Research:
(S)-(-)-1,2-Epithiododecane is used as a compound of interest in biology and pharmaceutical research because of its antimicrobial properties, which may contribute to the development of new antibiotics or antifungal agents.
Used in the Development of New Antibiotics:
In the pharmaceutical industry, (S)-(-)-1,2-Epithiododecane is used as a potential precursor for new antibiotics, given its antimicrobial properties.
Used in the Development of New Antifungal Agents:
Similarly, in the pharmaceutical industry, this compound is used as a potential precursor for new antifungal agents, again due to its antimicrobial characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 308103-61-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,8,1,0 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 308103-61:
(8*3)+(7*0)+(6*8)+(5*1)+(4*0)+(3*3)+(2*6)+(1*1)=99
99 % 10 = 9
So 308103-61-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H24S/c1-2-3-4-5-6-7-8-9-10-12-11-13-12/h12H,2-11H2,1H3/t12-/m0/s1
308103-61-9Relevant articles and documents
Mild and efficient desulfurization of thiiranes with MoCl5/Zn system
Yoo, Byung Woo,Lee, Yeong Jin,Shin, Jeong Won
, p. 124 - 131 (2021/11/10)
Desulfurization of a variety of thiiranes to alkenes occurs chemoselectively in high yields upon treatment with MoCl5/Zn system under mild conditions. The new methodology demonstrates high functional group tolerance toward chloro, bromo, fluoro, methoxy, ester, ether and keto groups.
Convenient procedure for converting 1,3-dithiolane-2-thiones into 1,3-dithiolan-2-ones
Barbero, Margherita,Degani, Iacopo,Dughera, Stefano,Fochi, Rita,Piscopo, Laura
, p. 289 - 294 (2007/10/03)
1,3-Dithiolan-2-ones have been obtained by reaction of 1,3-dithiolane-2-thiones and epoxides in the presence of HBF4·Et2O. The reactions, carried out in anhydrous CH2Cl2 at 0-5°C→room temperature (Procedure A) or in anhydrous chlorobenzene at 0-5→80°C (Procedure B), gave product yields of 63-95%. By Procedure B it was also possible to isolate the intermediates 1-oxa-4,6,9-trithiaspiro[4,4]nonanes in good yields (66-85%). Reaction pathways are proposed.
Silica Gel Assisted Synthesis of Thiiranes
Brimeyer, Michael O.,Mehrota, Ashok,Quici, Silvio,Nigam, Alok,Regen, Steven L.
, p. 4254 - 4255 (2007/10/02)
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