10250-52-9 Usage
Uses
Used in Pharmaceutical Industry:
Propylidene diiodide is used as a reagent for the preparation of pharmaceutical intermediates. It aids in the synthesis of various organic compounds that are essential in the development of pharmaceutical products.
Used in Agricultural Chemical Industry:
Propylidene diiodide is used as a reagent in the preparation of agricultural chemicals. It contributes to the synthesis of organic compounds that are vital in the production of agrochemicals for crop protection and enhancement.
Used in Organic Synthesis:
Propylidene diiodide is used as a reagent for the synthesis of various types of organic compounds, including alkenes, alkynes, and aromatic compounds. Its high reactivity makes it a valuable component in the creation of complex organic molecules.
Used in Functional Materials and Polymers Synthesis:
Propylidene diiodide serves as a precursor for the synthesis of functional materials and polymers. Its unique properties allow for the development of advanced materials with specific applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 10250-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,5 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10250-52:
(7*1)+(6*0)+(5*2)+(4*5)+(3*0)+(2*5)+(1*2)=49
49 % 10 = 9
So 10250-52-9 is a valid CAS Registry Number.
10250-52-9Relevant academic research and scientific papers
Nucleophilic and electrophilic properties of diiodomethyl lithium and sodium
Charreau, P.,Julia, M.,Verpeaux, J. N.
, p. 275 - 282 (2007/10/02)
The previously unreported diiodomethylsodium has been prepared; its thermal stability as well as nucleophilc behaviour (alkylation leading to 1,1-diiodoalkanes and allylation leading either to 1,1-diiodo-3-alkenes or 1-iodoalkadiene) are described and compared with the corresponding reactions of the lithium carbenoid.Alternatively, both lithium and sodium derivatives of diiodomethane react as electrophiles with α-sulfonyl carbanions to give 1-iodoalkenes in good yield.
Synthesis of 1,1-Dihaloalkanes
Garcia Martinez, A.,Herrera Fernandez, A.,Martinez Alvarez, R.,Garcia Fraile, A.,Bueno Calderon, J.,et al.
, p. 1076 - 1078 (2007/10/02)
The reaction of 1,1-bistrifluoromethylsulfonyloxy-alkanes (2) with magnesium iodide in carbon disulphide at O deg C affords 1,1-diiodoalkanes (3-I) in good yields.No rearrangement products are observed.The reaction of 2 with magnesium bromide in carbon disulphide or titanium tetrachloride in dichloromethane yields either 1,1-dichloro- (3-Cl) or 1,1-dibromoalkanes (3-Br).Rearrangements products are formed from α-branched substrates.
