1769-52-4 Usage
Uses
Used in Organic Synthesis:
2,3-dihydro-1H-phosphole is used as a building block in organic synthesis for the creation of more complex molecules. Its ability to form stable complexes and its reactivity with other compounds make it a valuable component in the synthesis of advanced organic molecules.
Used in Coordination Chemistry:
In coordination chemistry, 2,3-dihydro-1H-phosphole is used as a ligand, particularly in the formation of metal complexes. Its capacity to bind with metal ions enhances the stability and properties of these complexes, which is crucial in various chemical reactions and applications.
Used in Pharmaceutical Industry:
2,3-dihydro-1H-phosphole is utilized as a key component in the development of pharmaceuticals. Its unique structure allows it to interact with biological targets, making it a promising candidate for the design of new drugs with specific therapeutic effects.
Used in Agrochemicals:
In the agrochemical industry, 2,3-dihydro-1H-phosphole is employed for the synthesis of compounds with pesticidal properties. Its ability to form stable complexes with metal ions contributes to the development of effective and environmentally friendly agrochemicals.
Used in Materials Science:
2,3-dihydro-1H-phosphole also finds applications in materials science, where it is used to develop new materials with specific properties. Its versatility in forming complexes and its unique structure make it a valuable component in the creation of advanced materials for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1769-52-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,6 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1769-52:
(6*1)+(5*7)+(4*6)+(3*9)+(2*5)+(1*2)=104
104 % 10 = 4
So 1769-52-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H7P/c1-2-4-5-3-1/h1,3,5H,2,4H2
1769-52-4Relevant academic research and scientific papers
Harthcock, M. A.,Villarreal, J. R.,Richardson, L. W.,Laane, J.
, p. 1365 - 1368 (1984)
The far-infrared and low-frequency Raman spectra of 2-phospholene, , and 2-phospholene-1-d have been recorded.Four infrared and three Raman ring-puckering transitions were observed for each isotopic species.Kinetic energy expansions, corresponding to reduced masses of 130.42 and 136.72 au, were calculated for the two species, and these were used to determine the asymmetric potential function for the ring puckering vibration of molecules: V(cm-1) = 6.05 X 1E5x4 + 3.24 X 1E5x3 + 5.43 X 1E4x2, where x is the puckering coordinate in angstroms.The minimum at x = 0 corresponds to a puckered (presumably endo) conformation.Inflection points occur in the potential function at x = -0.08 Angstroem (where V = 205 cm-1) and x = -0.19 Angstroem (where V = 524 cm-1).It is likely that the less stable planar ring conformation and the less stable puckered conformation (exo) may be associated with these values.
