2510-89-6 Usage
General Description
Dipropyl chlorophosphate is an organophosphate compound that is commonly used as a chemical intermediate in the production of insecticides, herbicides, and flame retardants. It is often utilized as a pesticide and has been shown to have high toxicity in both acute and chronic exposures. Dipropyl chlorophosphate is a colorless to light yellow liquid with a pungent odor and can be very harmful if inhaled, ingested, or comes into contact with the skin. It is important to handle this chemical with caution and adhere to safety guidelines to prevent any potential health risks. Furthermore, due to its potential toxicity, it is crucial to properly dispose of any waste containing dipropyl chlorophosphate to avoid environmental contamination.
Check Digit Verification of cas no
The CAS Registry Mumber 2510-89-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,1 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2510-89:
(6*2)+(5*5)+(4*1)+(3*0)+(2*8)+(1*9)=66
66 % 10 = 6
So 2510-89-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H14ClO3P/c1-3-5-9-11(7,8)10-6-4-2/h3-6H2,1-2H3
2510-89-6Relevant articles and documents
Reaction of Thiolo and Selenolo Esters of Phosphorus Acids with Halogens. Part 3. Interaction of O,O,S-Trialkyl Phosphorothioates and O,S-Dialkyl t-Butylphosphonothioates with Sulphuryl Chloride and Halogens
Krawiecka, Bozena,Wojna-Tadeusiak, Elzbieta
, p. 229 - 237 (2007/10/02)
The reaction of the title phosphono- and phosphoro-thiolates with sulphuryl chloride and halogens involves in every case the formation of intermediates containing two phosphorus atoms >P+(SR)OP(O)- (X = SO2Cl or halogen).The formation of the latter in the course of chlorinolysis of phosphorus thiolesters is suggested to be responsible for the occurrence of a mechanism involving retention of configuration.The effect of the structure of the reactants and the nature of solvent on the reaction stereochemistry is discussed.
