32162-29-1 Usage
Uses
Used in Organic Synthesis:
(1alpha,2alpha,5alpha)-6,6-dimethylspiro[bicyclo[3.1.1]heptane-2,2'-oxirane] is used as a synthetic intermediate for the preparation of various complex organic molecules. Its unique structure and reactivity with nucleophiles or electrophiles make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (1alpha,2alpha,5alpha)-6,6-dimethylspiro[bicyclo[3.1.1]heptane-2,2'-oxirane] is used as a key component in the development of new drugs. Its chiral centers and oxirane ring can be exploited to create enantiomerically pure compounds with potential therapeutic applications. (1alpha,2alpha,5alpha)-6,6-dimethylspiro[bicyclo[3.1.1]heptane-2,2'-oxirane] may also serve as a precursor for the synthesis of biologically active molecules with novel mechanisms of action.
Used in Materials Science:
(1alpha,2alpha,5alpha)-6,6-dimethylspiro[bicyclo[3.1.1]heptane-2,2'-oxirane] is utilized in materials science for the development of advanced materials with unique properties. Its rigid bicyclic structure and oxirane ring can be incorporated into polymers, coatings, and other materials to impart specific characteristics, such as improved mechanical strength, thermal stability, or chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 32162-29-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,1,6 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 32162-29:
(7*3)+(6*2)+(5*1)+(4*6)+(3*2)+(2*2)+(1*9)=81
81 % 10 = 1
So 32162-29-1 is a valid CAS Registry Number.
32162-29-1Relevant academic research and scientific papers
Cyclobutane Ring Opening of Pin-2(10)-ene with Mercury(II) Salts. A New, High-yield Synthesis of p-Mentha-1,8-dien-7-ol
Bluthe, Norbert,Ecoto, Jules,Fetizon, Marcel,Lazare, Sylvain
, p. 1747 - 1751 (2007/10/02)
The nucleophilic attack of pin-2(10)-ene-mercury(II) complex systems by water results in the opening of the four-membered ring leading to an allylic organomercury(II) derivative (11) with the p-menthane skeleton.This intermediate can be reduced by hydride to p-menth-1(2)-en-8-ol (6a) or can undergo an in situ SE2' elimination yielding p-menth-1(7)-en-8-ol (9a), in high yields. (-)-2,10-Epoxypinane (15) reacts with mercury(II) salts at room temperature, giving the diol (16) in a quantitative yield.Compound (16) is a suitable intermediate for convenient preparation of p-mentha-1,8-dien-7-ol (17) and its derivatives.
