244076-29-7 Usage
Stereochemical designation
(2R,3R)-rel-(9CI)
This indicates the spatial arrangement of the atoms in the molecule, specifically the configuration at the 2nd and 3rd carbon atoms.
Molecular structure
Contains sulfur, phosphorus, nitrogen, carbon, hydrogen, and oxygen atoms
The compound is composed of these elements, which contribute to its unique properties and reactivity.
Potential applications
Pharmaceuticals, agrochemicals, and materials science
Due to its complex structure, the compound may have uses in various industries, including the development of new drugs, pesticides, and materials.
Research interest
Academic researchers
The compound's unique properties and potential applications make it an interesting subject for academic research.
Handling and evaluation
Requires careful handling and evaluation
Due to its complex nature and potentially hazardous properties, the compound should be handled with caution and evaluated thoroughly before any applications can be pursued.
Chemical compound
Complex organic compound
The compound is classified as an organic compound, which means it primarily consists of carbon and hydrogen atoms, along with other elements like sulfur, phosphorus, nitrogen, and oxygen.
Check Digit Verification of cas no
The CAS Registry Mumber 244076-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,4,0,7 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 244076-29:
(8*2)+(7*4)+(6*4)+(5*0)+(4*7)+(3*6)+(2*2)+(1*9)=127
127 % 10 = 7
So 244076-29-7 is a valid CAS Registry Number.
244076-29-7Relevant articles and documents
Intramolecular cyclization of ω-haloalkylsubstituted thiophosphorylacetonitriles: Synthesis and stereochemistry of 3-cyano-2-oxo-1,2-thiaphosphacyclanes
Odinets, Irene L.,Vinogradova, Natalya M.,Lyssenko, Konstantin A.,Antipin, Michail Yu.,Petrovskii, Pavel V.,Mastryukova, Tatyana A.
, p. 1 - 21 (2007/10/03)
Intramolecular S-alkylation in a series of ω-haloalkyl-substituted thiophosphorylacetonitriles 5-7 presents an effective synthetic route to the hitherto unknown 3-cyano-2-oxo-1,2-thiaphospholanes 14 and thiaphosphinanes 15. The compounds were obtained as a mixture of cis- and trans-isomers that were resolved to individual stereoisomers in most cases. For some of them, X-ray diffraction analysis has been performed. It was shown that 31P NMR spectroscopy can be used to assign the stereochemistry of 3-cyano-2-oxo-1,2-thiaphosphacyclanes.
