68641-49-6 Usage
Description
Bis(2-oxo-3-oxazolidinyl)phosphinic chloride is a white solid chemical compound that is characterized by its unique structure and properties. It is a versatile molecule with potential applications in various fields due to its reactivity and stability.
Uses
Used in Pharmaceutical Industry:
Bis(2-oxo-3-oxazolidinyl)phosphinic chloride is used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly in the preparation of hexadepsipeptides. These hexadepsipeptides have potential applications in the development of new drugs and therapies.
Used in Chemical Synthesis:
In the field of chemical synthesis, Bis(2-oxo-3-oxazolidinyl)phosphinic chloride serves as a valuable building block for the creation of complex organic molecules. Its unique reactivity allows for the formation of diverse chemical structures, making it a useful tool in the synthesis of specialty chemicals and materials.
Used in Research and Development:
Due to its unique properties and potential applications, Bis(2-oxo-3-oxazolidinyl)phosphinic chloride is also utilized in research and development settings. Scientists and researchers can explore its properties and reactivity to develop new methodologies and applications in various industries, including pharmaceuticals, materials science, and chemical engineering.
Check Digit Verification of cas no
The CAS Registry Mumber 68641-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,6,4 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68641-49:
(7*6)+(6*8)+(5*6)+(4*4)+(3*1)+(2*4)+(1*9)=156
156 % 10 = 6
So 68641-49-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H8ClN2O5P/c7-15(12,8-1-3-13-5(8)10)9-2-4-14-6(9)11/h1-4H2
68641-49-6Relevant articles and documents
2-Naphthol as a powerful chromophore for the configurational assignment of carboxylic acid groups via the CD exciton chirality method
Hartl, Michaela,Humpf, Hans-Ulrich
, p. 1741 - 1747 (2000)
A novel approach for the stereochemical assignment of carboxylic acid groups via the circular dichroism (CD) exciton chirality method using the 2- naphthyl chromophore is described. Direct esterification of carboxyl groups with 2-naphthol was effectively achieved with the employment of N,N-bis[2- oxo-3-oxazolidinyl]phosphorodiamidic chloride as the activating reagent. The method was tested with several model compounds, including both cyclic and acyclic dicarboxylic acids, and also applied to the natural product abietic acid. (C) 2000 Elsevier Science Ltd.
Non-Imuunosuppressive cyclosporins and their use in the prevention and treatment of HIV infection
-
, (2008/06/13)
Disclosed are cyclosporin analogs having amino acid residue substitutions at positions 1, 3, or 7 of the cyclosporin peptide backbone. Also disclosed are conjugates of these cyclosporin analogs in which an HIV protease inhibitor moiety is conjugated to the position-7 amino acid residue of the cyclosporin. These compounds simultaneously bind to and inhibit cyclophilin and HIV protease. The compounds have good bioavailability and potent HIV inhibitory activity. They are useful in the treatment and prevention of HIV-mediated disorders, including AIDS.
Convenient Synthesis of Carboxylic Acid Anhydrides using N,N-Bisphosphorodiamidic Chloride
Cabre-Castellvi, J.,Palomo-Coll, A.,Palomo-Coll, A.L.
, p. 616 - 620 (2007/10/02)
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