60190-78-5 Usage
Description
Acetic acid, diazo(dimethoxyphosphinyl)-, methyl ester is a chemical compound with the molecular formula C4H9O4NP. It is a methyl ester of diazo(dimethoxyphosphinyl)acetic acid, known for its diazo group containing two methoxyphosphinyl groups. This colorless to pale yellow liquid with a pungent odor is highly flammable and potentially hazardous, necessitating careful handling.
Uses
Used in Organic Synthesis:
Acetic acid, diazo(dimethoxyphosphinyl)-, methyl ester is used as a reagent in organic synthesis for the preparation of phosphorus-based compounds. Its unique structure and reactivity make it a valuable component in creating various complex organic molecules.
Used in Research Applications:
In the research field, this compound is utilized for studying the properties and reactions of diazo and phosphorus-containing compounds. It aids in understanding the mechanisms and applications of such compounds in chemical reactions and processes.
Used in Industrial Applications:
Acetic acid, diazo(dimethoxyphosphinyl)-, methyl ester is employed in industrial settings for the production of specific chemicals and materials that require its distinctive properties. Its use in these applications is carefully managed to mitigate potential health and environmental risks.
It is important to handle Acetic acid, diazo(dimethoxyphosphinyl)-, methyl ester with caution due to its potential health and environmental risks, ensuring that safety protocols are strictly followed in research and industrial settings.
Check Digit Verification of cas no
The CAS Registry Mumber 60190-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,9 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60190-78:
(7*6)+(6*0)+(5*1)+(4*9)+(3*0)+(2*7)+(1*8)=105
105 % 10 = 5
So 60190-78-5 is a valid CAS Registry Number.
60190-78-5Relevant articles and documents
Total synthesis and structural confirmation of (±)-cuevaene A
Craven, Philip G.E.,Taylor, Richard J.K.
, p. 5422 - 5425 (2012)
The total synthesis and structural reassignment of cuevaene A have been completed. The key synthetic steps in the total synthesis included a base-promoted double conjugate addition and further elaboration to generate the tricyclic core structure, followed by construction of the trienoic acid side chain. Detailed comparison of proton and carbon NMR data with published values enabled the connectivity of the natural product, which had been debated in earlier publications, to be confirmed.
