70063-48-8 Usage
Uses
Used in Pharmaceutical Industry:
2-(dichloromethylidene)-1,3-dithiane is used as a synthetic intermediate for the production of various pharmaceuticals. Its reactivity allows for the creation of complex molecules that can be used in the development of new drugs and medicines.
Used in Agrochemical Industry:
2-(dichloromethylidene)-1,3-dithiane is used as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its ability to form a wide range of compounds makes it a valuable component in the development of effective agricultural products.
Used in Research and Development:
2-(dichloromethylidene)-1,3-dithiane is used as a research tool in the field of organic chemistry. Its reactivity and ability to form various compounds make it an essential component in the exploration of new chemical reactions and the synthesis of novel molecules.
Used in Industrial Processes:
2-(dichloromethylidene)-1,3-dithiane is used as a key component in the production of high-value products in various industries. Its versatility and reactivity contribute to the development of innovative materials and compounds with potential applications in a wide range of sectors. Due to its reactivity, it should be handled with care and used in a well-ventilated area to ensure safety during its application in these processes.
Check Digit Verification of cas no
The CAS Registry Mumber 70063-48-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,0,6 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 70063-48:
(7*7)+(6*0)+(5*0)+(4*6)+(3*3)+(2*4)+(1*8)=98
98 % 10 = 8
So 70063-48-8 is a valid CAS Registry Number.
70063-48-8Relevant academic research and scientific papers
A Variable Mechanism for the Nucleophilic Vinylic Substitutions in a Series of gem-Dihalogenated Alkenes by a Bidentate Sulfur Nucleophile: An Experimental and AM1 Theoretical Study
Gimbert, Yves,Moradpour, Alec,Dive, Georges,Dehareng, Dominique,Lahlil, Khaled
, p. 4685 - 4690 (2007/10/02)
The nucleophilic substitutions of a series of gem-dihalogenated alkenes 3, 5, 7, 8, and 9 (RS)2C=CX2 (X = Cl, F) with 1,2-benzenedithiolate b have been studied.Depending on the structures of the R groups (alkyl, saturated and unsaturated cycloalkyls, aromatic ring), the course of the reactions and the structures of the yielded products are modified.In the frame of the addition-elimination-type mechanism for these nucleophilic substitutions, the energy contents of the anionic intermediates, resulting from the additions of the nucleophile b to the unsaturated centers,is calculated at the AM1 method level.For the compounds 5, 7, 8, and 9, the calculated energies nicely corroborate the experimental results.For 3, anionic intetrmediates are no longer found by calculation, and a synchronous single-step substitution is strongly suggested.
