33927-41-2 Usage
Chemical structure
Cyclic amide with a dithiane ring and a carboxamide group
The compound has a cyclic structure, with a dithiane ring (a six-membered ring containing two sulfur atoms) and a carboxamide group (a carbonyl group attached to an amide group).
Derivative of dithiane
Yes
1,3-Dithiane-2-carboxamide(9CI) is derived from dithiane, which is a sulfur-containing heterocyclic compound.
Common use
Protecting group in organic synthesis
Dithiane and its derivatives, including 1,3-Dithiane-2-carboxamide(9CI), are often used as protecting groups in organic synthesis to shield functional groups from unwanted reactions.
Potential applications
Medicinal chemistry and organic synthesis
The unique structural features and reactivity of 1,3-Dithiane-2-carboxamide(9CI) make it a candidate for various applications in medicinal chemistry and organic synthesis.
Possible use
Development of pharmaceuticals
Due to its properties, 1,3-Dithiane-2-carboxamide(9CI) may be useful in the development of new pharmaceuticals.
Possible use
Building block in the synthesis of important organic compounds
The compound may serve as a building block for the synthesis of other important organic compounds.
Further research needed
Yes
More research is required to fully explore the potential uses and properties of 1,3-Dithiane-2-carboxamide(9CI).
Check Digit Verification of cas no
The CAS Registry Mumber 33927-41-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,9,2 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 33927-41:
(7*3)+(6*3)+(5*9)+(4*2)+(3*7)+(2*4)+(1*1)=122
122 % 10 = 2
So 33927-41-2 is a valid CAS Registry Number.
33927-41-2Relevant academic research and scientific papers
Gaggero,Colonna,Albanese,Ottolina,Del Monte
, p. 1332 - 1339 (2009)
Two enzyme-mediated methods are presented for the preparation of enantiomerically enriched C2 1,3-dithiane-1,3-dioxide. The first takes advantage of a trans stereoselective oxidation by NaIO4 of enantiomerically pure (R) 1,3-dithiane-1-oxide ob
