695-59-0 Usage
Chemical classification
Phosphole oxide
A phosphorus-containing heterocyclic compound with a five-membered ring structure.
Usage
Different sources of media describe the Usage of 695-59-0 differently. You can refer to the following data:
1. Ligand in coordination chemistry
It forms complexes with metal ions, enhancing the stability and reactivity of the metal center.
2. Catalyst in organic synthesis
It accelerates organic reactions, increasing the reaction rate and selectivity without being consumed in the process.
Molecular structure
Unique and versatile
The compound has a specific arrangement of atoms that allows it to participate in various chemical reactions, particularly in the formation of metal complexes and catalyzing organic reactions.
Stability
High
The compound's structure contributes to its stability, making it suitable for use in various chemical reactions and applications in organic and coordination chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 695-59-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 695-59:
(5*6)+(4*9)+(3*5)+(2*5)+(1*9)=100
100 % 10 = 0
So 695-59-0 is a valid CAS Registry Number.
695-59-0Relevant articles and documents
Esterification of five-membered cyclic phosphinic acids under mild conditions using propylphosphonic anhydride (T3P)
Jablonkai, Erzsébet,Milen, Mátyás,Drahos, László,Keglevich, Gy?rgy
, p. 5873 - 5875 (2013/10/21)
1-Hydroxy-phospholene 1-oxides (1 and 3) and 1-hydroxy-phospholane oxides (5 and 7) undergo fast and efficient esterification with a series of alcohols, at room temperature, in the presence of 1.1 equiv of propylphosphonic anhydride (T3P).
Ring Expansion in the Addition of Dichlorocarbene to 2,5-Dihydro-1H-phosphole 1-Oxides
Keglevich, Gyoergy,Petnehazy, Imre,Miklos, Peter,Almasy, Attila,Toth, Gabor,et al.
, p. 3983 - 3986 (2007/10/02)
While the addition of dichlorocarbene to 2,5-dihydro-3-methyl-1H-phosphole 1-oxides (1a-d) carried out under phase-transfer catalytic conditions gave 6,6-dichloro-1-methyl-3-phosphabicyclohexane 1-oxides (2a-d), the 3,4-dimethyl-1-phenyl analogue (
SYNTHESIS AND STRUCTURE OF NITROPHOSPHOLENONE OXIMES
Berestovitskaya, V. M.,Efremov, D. A.,Berkova, G. A.,Perekalin, V. V.
, p. 2084 - 2092 (2007/10/02)
1.Nitration of 1-oxo-1-alkoxy-3-phospholenes and 1-oxo-1-alkoxy-3-methyl-4-phospholenes with nitrogen tetroxide yields a series of 1-oxo-1-alkoxy-2-oximino-4-nitro-3-phospholenes, which are the first reported nitro derivatives of organophosphorus oximes.T
