74095-34-4 Usage
Uses
Used in Industrial and Agricultural Applications:
(3-Pyridinylmethyl)phosphonic acid is used as a chelating agent for metal ion sequestration and water treatment. Its ability to bind to metal ions helps in managing metal ion concentrations in various industrial processes and agricultural settings.
Used in Pharmacological Applications:
(3-Pyridinylmethyl)phosphonic acid is used as a potential therapeutic agent for metal ion-related diseases. Its metal-binding capability allows it to target and treat conditions associated with metal ion imbalances or toxicity.
Used in Chemical Synthesis:
(3-Pyridinylmethyl)phosphonic acid is used as a building block in the synthesis of coordination compounds. Its structural features make it a valuable component in creating new compounds with specific properties and applications.
Used in Catalysis in Organic Synthesis:
(3-Pyridinylmethyl)phosphonic acid is used as a catalyst in organic synthesis processes. Its ability to bind and activate metal ions can enhance the efficiency and selectivity of various chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 74095-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,0,9 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74095-34:
(7*7)+(6*4)+(5*0)+(4*9)+(3*5)+(2*3)+(1*4)=134
134 % 10 = 4
So 74095-34-4 is a valid CAS Registry Number.
74095-34-4Relevant academic research and scientific papers
Okamoto, Yoshiki,Kokubo, Ichiro,Takamuku, Setsuo
, p. 2438 - 2440 (1990)
Upon UV-irradiation, the C-P bond of (4-pyridylmethyl)phosphonic acid cleaved only near the isoelectronic point to give 4-methylpyridinium phophate, while (1-benzyl-4-pyridiniomethyl)phosphonic acid underwent C-P bond cleavage above pH 4 to give 1-benzyl-4-methylpyridinium phosphate.On the other hand, the C-P bond of (2-pyridylmethyl)phosphonic acid cleaved under pH region of about 1 to 2, while (1-benzyl-2-pyridiniomethyl)phosphonic acid underwent C-P bond cleavage above pH4.
