114028-43-2 Usage
Molecular Weight
257.38 g/mol The mass of one mole of the chemical.
Physical State
Colorless liquid The chemical is a liquid that is colorless in appearance.
Solubility
Insoluble in water The chemical does not dissolve well in water.
Vapor Pressure
1.25 mm Hg at 25°C The chemical has a vapor pressure of 1.25 millimeters of mercury at a temperature of 25 degrees Celsius, indicating that it does not easily evaporate at room temperature.
Uses
Industrial applications (production of polymers, dyes, and pharmaceuticals), solvent, intermediate in the synthesis of other compounds The chemical is used in a variety of industrial applications, including the production of polymers, dyes, and pharmaceuticals. It is also used as a solvent and as an intermediate in the synthesis of other compounds.
Toxicity
Toxic if swallowed, irritating to the skin and respiratory system, may cause long-term effects in aquatic environments The chemical can be harmful if ingested and may cause irritation to the skin and respiratory system. It may also have negative effects on aquatic life if not handled properly.
Check Digit Verification of cas no
The CAS Registry Mumber 114028-43-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,0,2 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 114028-43:
(8*1)+(7*1)+(6*4)+(5*0)+(4*2)+(3*8)+(2*4)+(1*3)=82
82 % 10 = 2
So 114028-43-2 is a valid CAS Registry Number.
114028-43-2Relevant articles and documents
Pathways of Pd-catalyzed cyclopropanation of tetrahydroindene with diazomethane
Menchikov, Leonid G.,Pantyukh, Olga A.,Shulishov, Evgeny V.,Tomilov, Yury V.
, p. 612 - 614 (2020/10/09)
The Pd-catalyzed cyclopropanation of 3a,4,7,7a-tetrahydro-1H-indene with diazomethane unexpectedly affords monoand dicyclopropanation products in good yields, the cyclopentene double bond being approximately three times more reactive than the cyclohexene one. In contrast, similar independent competitive cyclopropanation of a cyclopentene–cyclohexene mixture has shown that cyclohexene exhibits an abnormally low reactivity differing by about two orders of magnitude.
POLYCYCLIC AND FRAMEWORK COMPOUNDS. XIV. REACTION OF DICHLOROCARBENE WITH endo-TRICYCLO2,6>DECA-3,8-DIENE
Kazimirchik, I. V.,Lukin, K. A.,Borisenko, A. A.,Bebikh, G. F.,Yarovoi, S. S.,Zefirov, N. S.
, p. 507 - 512 (2007/10/02)
The addition of dichlorocarbene in a two-phase system to endo-tricyclo2,6>deca-3,8-diene leads to the formation of either 4,4-dichlorotetracyclo2,703,5>undec-9-ene or isomeric tetrachlorotetracyclo6.3.1.0
