61128-73-2 Usage
Uses
Used in Organic Synthesis:
TETRAHYDRO-PYRAN-4-ONE OXIME is used as a building block for the synthesis of various organic compounds, providing a versatile starting material for the creation of complex molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, TETRAHYDRO-PYRAN-4-ONE OXIME is used as a reagent in the preparation of heterocyclic compounds, which are often found in many drug molecules, contributing to their therapeutic properties.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, TETRAHYDRO-PYRAN-4-ONE OXIME is employed as a reagent for the synthesis of heterocyclic compounds that are utilized in the development of pesticides and other agricultural chemicals.
Used as a Chelating Agent:
TETRAHYDRO-PYRAN-4-ONE OXIME is used as a chelating agent to form stable complexes with metal ions, which is beneficial in various applications such as in the purification of metal solutions or in the synthesis of metal-organic frameworks.
Check Digit Verification of cas no
The CAS Registry Mumber 61128-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,1,2 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61128-73:
(7*6)+(6*1)+(5*1)+(4*2)+(3*8)+(2*7)+(1*3)=102
102 % 10 = 2
So 61128-73-2 is a valid CAS Registry Number.
61128-73-2Relevant academic research and scientific papers
New acyloxy nitroso compounds with improved water solubility and nitroxyl (HNO) release kinetics and inhibitors of platelet aggregation
Mohamed, Heba A.H.,Abdel-Aziz, Mohamed,Abuo-Rahma, Gamal El-Din A.A.,King, S. Bruce
, p. 6069 - 6077 (2015/11/10)
New acyloxy nitroso compounds, 4-nitrosotetrahydro-2H-pyran-4-yl 2,2,2-trichloroacetate and 4-nitrosotetrahydro-2H-pyran-4-yl 2,2-dichloropropanoate were prepared. These compounds release HNO under neutral conditions with half-lives between 50 and 120 min, identifying these HNO donors as kinetically intermediate to the much slower acetate derivative and the faster trifluoroacetic acid derivative. These compounds or HNO-derived from these compounds react with thiols, including glutathione, thiol-containing enzymes and heme-containing proteins in a similar fashion to other acyloxy nitroso compounds. HNO released from these acyloxy nitroso compounds inhibits activated platelet aggregation. These acyloxy nitroso compounds augment the range of release for this group of HNO donors and should be valuable tools in the further study of HNO biology.
