2510-89-6 Usage
Uses
Used in Pesticide Industry:
Dipropyl chlorophosphate is used as a pesticide for its effectiveness in controlling pests. Its high toxicity makes it a potent agent in eliminating insects that can cause damage to crops and other plants.
Used in Chemical Intermediates:
In the chemical industry, dipropyl chlorophosphate serves as an intermediate in the synthesis of various compounds, including insecticides, herbicides, and flame retardants. Its reactivity and versatility make it a valuable component in the production of these products.
Used in Flame Retardants:
Dipropyl chlorophosphate is used as a component in flame retardants to enhance the fire resistance of materials. Its chemical properties contribute to the effectiveness of these products in preventing the spread of flames and reducing the risk of fire-related incidents.
Safety Precautions:
Due to the high toxicity of dipropyl chlorophosphate, it is essential to handle this chemical with extreme caution. Proper safety measures, such as wearing protective gear and following safety guidelines, should be strictly adhered to during its use and storage. Additionally, any waste containing dipropyl chlorophosphate should be disposed of properly to prevent environmental contamination and potential health hazards.
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.