147441-52-9 Usage
Description
(2S)-2-(4-bromophenyl)-1,3-oxathiolane is a chiral chemical compound with the molecular formula C8H7BrOS. It features a six-membered heterocyclic ring composed of oxygen, sulfur, and carbon atoms, to which a bromophenyl group is attached at one of the carbon atoms. (2S)-2-(4-bromophenyl)-1,3-oxathiolane holds potential in pharmaceutical research and medicinal chemistry due to its unique structure and properties.
Uses
Used in Pharmaceutical Research:
(2S)-2-(4-bromophenyl)-1,3-oxathiolane is utilized as a key intermediate in the synthesis of various pharmaceutical agents. Its unique structure allows it to target specific biological pathways, making it a valuable component in drug development.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2S)-2-(4-bromophenyl)-1,3-oxathiolane serves as a building block for designing new molecules with therapeutic potential. Its versatility in chemical modifications contributes to the creation of diverse drug candidates for treating various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 147441-52-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,4,4 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 147441-52:
(8*1)+(7*4)+(6*7)+(5*4)+(4*4)+(3*1)+(2*5)+(1*2)=129
129 % 10 = 9
So 147441-52-9 is a valid CAS Registry Number.
147441-52-9Relevant articles and documents
Blue LED-Promoted Oxathiacetalization of Aldehydes and Ketones
Liu, You-Chen,Reddy, Daggula Mallikarjuna,Chen, Xin-An,Shieh, Yi-Chen,Lee, Chin-Fa
, p. 2542 - 2552 (2020/04/27)
In synthetic chemistry, the protection of aldehydes and ketones is crucial during multistep synthesis of complex molecules. Organic chemists have paid substantial attention to the synthesis of 1,3-oxathiolanes and 1,3-oxathianes because of their considera
Nickel(II) chloride hexahydrate catalyzed reaction of aromatic aldehydes with 2-mercaptoethanol: Formation of supramolecular helical assemblage of the product
Laskar, Rajibul A.,Begum, Naznin A.,Mir, Mohammad Hedayetullah,Rohman, Md. Rumum,Khan, Abu T.
, p. 5839 - 5844 (2013/10/21)
Various aromatic aldehydes on reaction with 2-mercaptoethanol provided an unanticipated product, bis(2-hydroxyethyl)dithioacetals (3) as the major product along with the expected product 1,3-oxathiolanes (4) in the presence of 0.05 equiv amount of nickel(
Melamine trisulfonic acid as a new, efficient and reusable catalyst for the chemoselective oxathioacetalyzation of aldehydes
Shirini,Albadi
experimental part, p. 1119 - 1120 (2010/09/10)
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