40928-00-5 Usage
Uses
Used in Organic Synthesis:
2-(propan-2-yloxy)-1,3,2-dioxaphospholane is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of new compounds and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(propan-2-yloxy)-1,3,2-dioxaphospholane is used as a ligand in coordination chemistry, which is crucial for the development of new drugs and pharmaceutical agents. Its unique properties allow it to bind with metal ions, enhancing the effectiveness and selectivity of certain drug candidates.
Used in Agricultural Industry:
2-(propan-2-yloxy)-1,3,2-dioxaphospholane is utilized in the agricultural sector for the production of agrochemicals and pesticides. Its role in these applications is to improve the efficiency and effectiveness of these products, ensuring better crop protection and yield.
Used in Chemical Intermediates Production:
2-(propan-2-yloxy)-1,3,2-dioxaphospholane is also used as a key intermediate in the synthesis of various specialty chemicals. Its presence in the production process allows for the creation of a wide range of chemical products with diverse applications in different fields.
Overall, 2-(propan-2-yloxy)-1,3,2-dioxaphospholane is a multifaceted chemical compound with significant applications in organic synthesis, pharmaceuticals, agriculture, and the production of chemical intermediates, showcasing its importance in the development of new materials and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 40928-00-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,2 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 40928-00:
(7*4)+(6*0)+(5*9)+(4*2)+(3*8)+(2*0)+(1*0)=105
105 % 10 = 5
So 40928-00-5 is a valid CAS Registry Number.
40928-00-5Relevant academic research and scientific papers
MECHANISM OF NUCLEOPHILIC SUBSTITUTION AT TRICOVALENT PHOSPHORUS
Dahl, Otto
, p. 201 - 204 (2007/10/02)
The mechanism of substitution reactions at tricovalent phosphorus, mainly the system + ROH, is discussed on the basis of stereochemistry, catalysis, kinetics and substituent effects.
