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Exo,endo-4,4-dichlorotetracyclo<6.2.1.03,5.02.7>undec-9-ene is a complex organic compound with a unique cyclic structure. It consists of four fused rings, with the molecular formula C11H12Cl2. The compound is characterized by the presence of two chlorine atoms attached to carbon atoms at positions 4 and 4', and a double bond at the 9th position. The exo,endo notation indicates the relative positions of the chlorine atoms and the double bond within the molecule. exo,endo-4,4-dichlorotetracyclo<6.2.1.03,5.02.7>undec-9-ene is of interest in organic chemistry due to its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its role as an intermediate in the production of other complex organic molecules.

3762-19-4

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3762-19-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3762-19-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,6 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3762-19:
(6*3)+(5*7)+(4*6)+(3*2)+(2*1)+(1*9)=94
94 % 10 = 4
So 3762-19-4 is a valid CAS Registry Number.

3762-19-4Relevant academic research and scientific papers

REACTIONS OF DICHLOROCARBENE AND OF THE SIMMONS-SMITH REAGENT WITH THE DIMER AND TRIMER OF CYCLOPENTADIENE AND THE DIMER OF SPIROHEPTA-4,6-DIENE

Molchanov, A. P.,Kostikov, R. R.,Chernyshev, V. A.

, p. 1444 - 1449 (2007/10/02)

Dichlorocarbene reacts with the exo dimer of cyclopentadiene (exo-tricyclo2,6>deca-3,8-diene) and the trimer of cyclopentadiene (exo-endo-pentacyclo2,7.09,13>pentadeca-4,10-diene) at the cyclopentene double bond.The Simmons-Smith reagent, prepared from methylene iodide in presence of a zinc-silver couple, reacts with the same hydrocarbons and also with the dimer of spirohepta-4,6-diene 2,6>deca-3,8-diene)-10-spirocyclopropane> nonselectively at both double bonds, whereas it adds to the trimer of cyclopentadiene only at the norbornene double bond.

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

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