5685-42-7 Usage
Uses
Used in Organic Chemistry:
1-(2,2-Dichlorocyclopropyl)hexane is utilized as a reagent in organic chemistry for a variety of reactions, including dichlorocyclopropane ring-opening processes. Its unique structure and properties make it a promising candidate for the synthesis of complex organic compounds, contributing to the development of novel materials and molecules.
Used in Agricultural Applications:
Within the agricultural industry, 1-(2,2-Dichlorocyclopropyl)hexane may find use as a component in the development of new products, potentially enhancing the properties of existing chemicals or creating new ones with improved performance. Its unique structure could provide valuable properties for agricultural applications, such as pest control or crop protection.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, 1-(2,2-Dichlorocyclopropyl)hexane holds potential for the development of new drugs and therapeutic agents. Its unique structure could be harnessed to create novel compounds with specific biological activities, potentially leading to the discovery of new treatments for various diseases and medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 5685-42-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,8 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5685-42:
(6*5)+(5*6)+(4*8)+(3*5)+(2*4)+(1*2)=117
117 % 10 = 7
So 5685-42-7 is a valid CAS Registry Number.
5685-42-7Relevant academic research and scientific papers
Formation of three-membered rings by SHi displacement. Reverse of cyclopropyl ring opening
Tanner, Dennis D.,Zhang, Liying,Hu, Li Qing,Kandanarachchi, Pramod
, p. 6818 - 6824 (2007/10/03)
The general methods, photoinitiated or peroxide-initiated free radical chain additions of halomethanes to olefins, yield 1,2-addition products at temperatures ranging from 20 to 100°C. At lower temperatures, -42 to -104°C, a competitive reaction, subsequent to the addition of CCl2X., yields alkylcyclopropanes. The reactions of 1-octene or 1-hexene and 1-methylcyclohexene with atomic hydrogen carried out in the presence of several transfer agents (CCl4, CCl3Br, CCl2Br2) initiate a radical chain addition of CCl2X. and yield cyclized materials resulting from the SHi displacement of halogen by a carbon-centered radical. The radical displacement of a halogen on carbon, the reverse of homolytic displacement on cyclopropyl carbon, is dominant at low temperatures. The rate constants for cyclization (kc) vs transfer with halomethane (kt) showed isokinetic temperatures of -46°C (CCl4, 1-hexene); -35°C (CCl4, 1-methylcyclohexene). The isokinetic temperatures for the reactions of the two substrates carried out in the presence of BrCCl3 were calculated as -204 °C (1-octene) and -109°C (1-methylcyclohexene).
