60478-96-8 Usage
General Description
1,5-Dimethyl-6,8-dioxabicyclo[3.2.1]octane, also known as tetramethyleneglycolide, is a chemical compound with a bicyclic structure containing two seven-membered rings and one five-membered ring. It is a cyclic acetal derivative and is commonly used as a building block in organic synthesis. 1,5-Dimethyl-6,8-dioxabicyclo[3.2.1]octane has various applications in the pharmaceutical and chemical industries, including as a monomer in the production of polymers and as a reagent in organic reactions. It is also used as a solvent and as a component in the formulation of various chemical products. Additionally, 1,5-Dimethyl-6,8-dioxabicyclo[3.2.1]octane has been studied for its potential pharmacological activities, such as its antiviral and antifungal properties. Overall, this chemical compound has versatile uses and plays an important role in the synthesis of various organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 60478-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,7 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 60478-96:
(7*6)+(6*0)+(5*4)+(4*7)+(3*8)+(2*9)+(1*6)=138
138 % 10 = 8
So 60478-96-8 is a valid CAS Registry Number.
60478-96-8Relevant articles and documents
SYNTHESIS OF THE PHEROMONES, (E)-3,7-DIMETHYL-2,7-OCTADIENYL PROPIONATE, (E)-3,7-DIMETHYL-2-OCTENE-1,8-DIOL AND FRONTALIN FROM A COMMON INTERMEDIATE
Dhokte, U. P.,Rao, A. S.
, p. 811 - 822 (2007/10/02)
Ketal ester 9 has been prepared in five steps from methyl levulinate 4 (scheme 1).The propionate 1, diol 2 and (+/-) frontalin 3 were prepared from ester 9 employing the routes shown in scheme 2,3 and 4 respectively.The branched chain alkenes 13 and 20 were prepared conveniently from the primary alcohols 11 and 10 following the procedure of S.Wolff.Triethyl phosphonopropionate 7 has been prepared by methylating triethylphosphonoacetate with methyl iodide in the presence of sodium hydride.
Decomposition of bicyclic endoperoxides: An isomorphous synthesis of frontalin via 1,5-dimethyl-6,7-dioxabicyclo[3.2.1]octane
Wilson, R. Marshall,Rekers, John W.
, p. 206 - 207 (2007/10/02)
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