56306-51-5 Usage
General Description
1,2,3,4-Tetrahydro-1,4-methanonaphthalene-2,3-dimethanol, also known as tetrahydromethanophenanthrene, is a chemical compound with the molecular formula C12H16O2. It is a white, crystalline solid with a melting point of 181-183°C. 1,2,3,4-TETRAHYDRO-1,4-METHANONAPHTHALENE-2,3-DIMETHANOL is commonly used in organic synthesis and pharmaceutical research as a building block for more complex chemical structures. Its unique molecular structure and functional groups make it an important intermediate in the production of various pharmaceuticals and agrochemicals. Additionally, it exhibits pharmacological properties and is being studied for its potential medicinal applications. Overall, 1,2,3,4-Tetrahydro-1,4-methanonaphthalene-2,3-dimethanol is a versatile compound with important applications in both the chemical and pharmaceutical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 56306-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,0 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56306-51:
(7*5)+(6*6)+(5*3)+(4*0)+(3*6)+(2*5)+(1*1)=115
115 % 10 = 5
So 56306-51-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H16O2/c14-6-12-10-5-11(13(12)7-15)9-4-2-1-3-8(9)10/h1-4,10-15H,5-7H2
56306-51-5Relevant articles and documents
A Concise Synthesis of the 2,3-Dimethylene-1,4-methano-1,2,3,4-tetrahydronaphthalene and its Reaction with Singlet Oxygen
Atasoy, Basri,Bayramoglu, Fatma,Hoekelek, Tuncer
, p. 5753 - 5764 (2007/10/02)
Palladium-catalyzed carbomethoxylation of benzonorbornadiene (7) yielded dimethyl-1,4-methano-1,2,3,4-tetrahydronaphthalene-2,3-dicarboxylate (9) which was transformed in three steps into 2,3-dimethylene-1,4-methano-1,2,3,4-tetrahydronaphthalene (4) in a high yield.Reaction of 4 with singlet oxygen resulted in the formation of epoxy-endoperoxide (12).X-ray crystallographic analysis demonstrated that epoxide ring is exo as methylene bridge.For the first time, the epoxy-endoperoxide formation from the "one pot" reaction of a diene with singlet oxygen was observed.The epoxy-endoperoxide formation mechanism was discussed.CoTTP (Cobalt(II)tetraphenylporphyrin) catalyzed rearrangement of epoxy-endoperoxide gave hydroxy-aldehyde (13) which was oxidized into dialdehyde (14).
