332345-27-4 Usage
Uses
Used in Pharmaceutical Industry:
5-Morpholinothiophene-2-carboxylic acid is used as a building block for the synthesis of pharmaceuticals due to its potential to contribute to the development of new drugs with diverse pharmacological activities. Its unique structure allows for the creation of compounds that can target a wide range of therapeutic areas.
Used in Agrochemical Industry:
5-Morpholinothiophene-2-carboxylic acid is used as a precursor in the development of agrochemicals, where its chemical properties can be harnessed to create effective compounds for agricultural applications, such as pesticides or herbicides.
Used in Medicinal Chemistry Research:
5-Morpholinothiophene-2-carboxylic acid is used as a molecular scaffold in medicinal chemistry research for the design of new drugs. Its structure provides a foundation for the attachment of various functional groups, enabling the exploration of novel chemical entities with potential therapeutic benefits.
Used in Drug Discovery and Development:
5-Morpholinothiophene-2-carboxylic acid is utilized in drug discovery and development processes, where its promising biological activities in preliminary studies make it a valuable candidate for further research and potential clinical applications.
Overall, 5-Morpholinothiophene-2-carboxylic acid is a versatile and promising chemical compound with applications spanning across various industries, particularly in the development of pharmaceuticals and agrochemicals, as well as in medicinal chemistry research and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 332345-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,2,3,4 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 332345-27:
(8*3)+(7*3)+(6*2)+(5*3)+(4*4)+(3*5)+(2*2)+(1*7)=114
114 % 10 = 4
So 332345-27-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO3S/c11-9(12)7-1-2-8(14-7)10-3-5-13-6-4-10/h1-2H,3-6H2,(H,11,12)
332345-27-4Relevant academic research and scientific papers
Nguyen, Son T.,Li, Bing,Peet, Norton P.
, p. 6056 - 6058 (2015)
We have previously attempted to prepare 5-(4-morpholinyl)-2-aminothiophene (3) by reducing 5-(4-morpholinyl)-2-nitrothiophene (2), to prepare a precursor for the preparation of thienyloxazolidinones as potential linezolid-like antibiotics. This strategy failed, but allowed us to define an interesting reductive aromatization reaction. We have now succeeded in producing thienyloxazolidinones using an alternative strategy, initiating from 5-(4-morpholinyl)thiophene-2-carboxaldehyde (8). This Letter describes the synthesis of thienyloxazolidinone 14, which is a key intermediate for the preparation of new oxazolidinone antibiotics with a thiophene core.
