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Exo-2,10-bornanediol is a cyclic organic compound with the molecular formula C10H18O2. It is a diol, meaning it contains two hydroxyl (-OH) groups, and is derived from the bornane ring system. The "exo" prefix indicates that the hydroxyl groups are located on the exterior of the ring structure. exo-2,10-Bornanediol is known for its unique stereochemistry and is used in various chemical syntheses, particularly in the preparation of complex organic molecules. It is also of interest in the field of organic chemistry due to its potential applications in the development of new pharmaceuticals and materials.

1925-39-9

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1925-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1925-39-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,2 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1925-39:
(6*1)+(5*9)+(4*2)+(3*5)+(2*3)+(1*9)=89
89 % 10 = 9
So 1925-39-9 is a valid CAS Registry Number.

1925-39-9Relevant academic research and scientific papers

Electrochemical Oxidation of Polycyclic Cyclopropanes and Camphene. Novel Synthesis of exo-5,5-Dimethyl-6-methylenebicycloheptan-2-ol (Nojigiku Alcohol)

Uchida, Toshikazu,Matsubara, Yoshiharu,Nishiguchi, Ikuzo,Hirashima, Tsuneaki,Ohnishi, Takashi,Kanehira, Koichi

, p. 2938 - 2943 (2007/10/02)

Anodic oxidation of tricyclene (1a) in acetic acid containing triethylamine, followed by hydrolysis, provides a facile and efficient synthesis of exo-5,5-dimethyl-6-methylenebicycloheptan-2-ol (2a), named "nojigiku alcohol", which was isolated from the essential oil of chrysanthemum japonese.Furthermore, a method for large-scale production of 2a starting from the readily available impure starting tricyclene (1a) has been developed by appropriate selection of reaction conditions.Similar electrooxidation of the related naturally occurring polycyclic methylcyclopropanes, cyclofenchene (1b) and longicyclene (1c), followed by hydrolysis also brought about stereo- and regioselective cleavage of carbon-carbon bonds of the cyclopropane rings to give the corresponding homoallylic alcohols 2b,c in good yields.

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