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Endo-2-chloro-1,3,3-trimethylbicyclo[2.2.1]heptane is a complex organic compound with the molecular formula C10H17Cl. It is a halogenated derivative of the bicyclic hydrocarbon known as norbornane, which has a unique bridged structure. endo-2-chloro-1,3,3-trimethylbicyclo<2.2.1>heptane is characterized by a chlorine atom attached to the endo position of the norbornane ring, which influences its chemical reactivity and physical properties. It is a colorless liquid with a pungent odor and is used in various chemical syntheses, particularly in the production of pharmaceuticals and other specialty chemicals. Due to its potential reactivity and the presence of chlorine, it is important to handle endo-2-chloro-1,3,3-trimethylbicyclo<2.2.1>heptane with care, following appropriate safety protocols.

3372-12-1

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3372-12-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3372-12-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,7 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3372-12:
(6*3)+(5*3)+(4*7)+(3*2)+(2*1)+(1*2)=71
71 % 10 = 1
So 3372-12-1 is a valid CAS Registry Number.

3372-12-1Relevant academic research and scientific papers

Surface-mediated reactions. 3. Hydrohalogenation of alkenes

Kropp, Paul J.,Daus, Kimberlee A.,Tubergen, Mark W.,Kepler, Keith D.,Wilson, Vincent P.,Craig, Stephen L.,Baillargeon, Michelle M.,Breton, Gary W.

, p. 3071 - 3079 (1993)

Appropriately prepared silica gel and alumina have been found to mediate the addition of HCl, HBr, and HI to alkenes. The technique has been rendered even more convenient by the use of various organic and inorganic halides that undergo hydrolysis in the presence of silica gel or alumina to generate hydrogen halides in situ. Under these conditions alkenes such as cycloheptene (1), 1-octene (7), and 3,3-dimethyl-1-butene (15), which react with HCl only very slowly in solution, underwent rapid addition. 1-Octene (7) underwent ionic addition of HBr without competing radical addition. 1,2-Dimethylcyclohexane (24) afforded the syn addition product 25c, which underwent equilibration with the thermodynamically more stable isomer 25t. A mechanism for surface-mediated addition/elimination is proposed involving a stepwise transfer of H+ and X- from or to the surface in syn fashion, as shown in Scheme II.

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