10502-30-4 Usage
Description
2,6-dichloro-9-thiabicyclo[3.3.1]nonane is a bicyclic organic compound with the molecular formula C8H12Cl2S. It features a chlorine atom at the 2nd and 6th positions, and a sulfur atom at the 9th position. This chemical compound is primarily utilized in organic synthesis as a building block for pharmaceuticals, agrochemicals, and other fine chemicals. It has also been investigated for its potential biological activities and serves as a valuable intermediate in the production of various compounds, as well as a reactant in the preparation of other complex organic molecules.
Uses
Used in Pharmaceutical Industry:
2,6-dichloro-9-thiabicyclo[3.3.1]nonane is used as a building block for the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique structure allows for the creation of diverse chemical entities with potential medicinal properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2,6-dichloro-9-thiabicyclo[3.3.1]nonane is employed as a starting material for the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness in controlling pests and weeds in agricultural settings.
Used in Organic Synthesis:
2,6-dichloro-9-thiabicyclo[3.3.1]nonane is used as an intermediate in the production of various compounds, playing a crucial role in the synthesis of complex organic molecules. Its presence in these molecules can impart unique chemical and physical properties, making it a valuable component in the creation of specialty chemicals.
Used in Research and Development:
2,6-dichloro-9-thiabicyclo[3.3.1]nonane is utilized in research and development settings for the exploration of its potential biological activities. Studies on this compound can lead to the discovery of new applications in the fields of medicine, agriculture, and other areas where its properties may be beneficial.
Check Digit Verification of cas no
The CAS Registry Mumber 10502-30-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,0 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10502-30:
(7*1)+(6*0)+(5*5)+(4*0)+(3*2)+(2*3)+(1*0)=44
44 % 10 = 4
So 10502-30-4 is a valid CAS Registry Number.
10502-30-4Relevant articles and documents
Thia-, Aza-, and selena[3.3.1]bicyclononane dichlorides: Rates vs internal nucleophile in anchimeric assistance
Accurso, Adrian A.,Cho, So-Hye,Amin, Asmarah,Potapov, Vladimir A.,Amosova, Svetlana V.,Finn
body text, p. 4392 - 4395 (2011/07/30)
Sulfur-, selenium-, and nitrogen-containing compounds bearing leaving groups in the β-position undergo facile substitution chemistry enabled by anchimeric assistance. Here we provide direct comparisons between such systems in the rigid bicyclo[3.3.1]nonane framework easily derived from 1,5-cyclooctadiene. For a series of dichloride electrophiles of this type, the relative reactivities were found to be Se ? (alkyl)N > S ≥ (propargyl)N > (phenyl)N, with the reaction rates at the two extremes differing by more than 3 orders of magnitude. For the N-alkyl case, substitution rates were largely independent of the trapping nucleophile but were strongly dependent on solvent, showing that the process is controlled by the formation of the high-energy three-membered cationic intermediate.
Transannular Reactions of Cycloalkenes, Cycloalkadienes and Cycloalkatrienes. VIII. The Electrophilic Addition of Pseudohalogenes to Cycloocta-1(Z),5(Z)-diene
Haufe, Guenter,Muehlstaedt, Manfred
, p. 89 - 92 (2007/10/02)
The reaction of cycloocta-1(Z),5(Z)-diene 5 with chlorothiocyanate is described.The main process is the normal anti-addition to produce trans-5-chloro-6-thiocyanato-(Z)-cyclooctene 6.In addition 2,6-dichloro-9-thiabicyclononane 7 and 2,6-dithiocyanato-9-thiabicyclononane 8 are obtained as products of a transannular reaction.
