181701-06-4 Usage
Uses
Used in Pharmaceutical Industry:
Cycloocta(1,2-f:3,4-f)bis(1,3)benzodioxol-5-ol, 5,6,7,8-tetrahydro-13,14-dimethoxy-6,7-dimethyl-, benzoate, (5R,6S,7S,13aS)is used as a pharmaceutical compound for its potential biological activities. Its unique structure may contribute to specific therapeutic effects, making it a candidate for drug development and research.
Used in Chemical Industry:
In the chemical industry, Cycloocta(1,2-f:3,4-f)bis(1,3)benzodioxol-5-ol, 5,6,7,8-tetrahydro-13,14-dimethoxy-6,7-dimethyl-, benzoate, (5R,6S,7S,13aS)is used as a chemical intermediate or building block for the synthesis of other complex organic compounds. Its specific stereochemistry and functional groups can be utilized in the development of novel chemical products with desired properties.
Due to the complexity and specific stereochemistry of Cycloocta(1,2-f:3,4-f)bis(1,3)benzodioxol-5-ol, 5,6,7,8-tetrahydro-13,14-dimethoxy-6,7-dimethyl-, benzoate, (5R,6S,7S,13aS)-, careful handling and thorough characterization are required before its application in any industry. This ensures the safety and effectiveness of the compound in its intended use.
Check Digit Verification of cas no
The CAS Registry Mumber 181701-06-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,7,0 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 181701-06:
(8*1)+(7*8)+(6*1)+(5*7)+(4*0)+(3*1)+(2*0)+(1*6)=114
114 % 10 = 4
So 181701-06-4 is a valid CAS Registry Number.
181701-06-4Relevant articles and documents
Asymmetric synthesis of the dibenzocyclooctadiene lignans interiotherin A and gomisin R
Coleman, Robert S.,Gurrala, Srinivas Reddy
, p. 1849 - 1852 (2005)
(Chemical Equation Presented) Asymmetric total syntheses of the dibenzocyclooctadiene lignans interiotherin A and angeloylgomisin R are reported. The syntheses were based on an atropdiastereoselective, copper-promoted biaryl coupling reaction, a diastereo
Asymmetric total synthesis of dibenzocyclooctadiene lignan natural products
Coleman, Robert S.,Gurrala, Srinivas Reddy,Mitra, Soumya,Raao, Amresh
, p. 8932 - 8941 (2007/10/03)
Full details of the asymmetric total syntheses of the dibenzocyclooctadiene lignans interiotherin A, angeloylgomisin R, gomisin O, and gomisin E (epigomisin O) are presented. The syntheses were based on a unified synthetic strategy involving a novel crotylation using the Leighton auxiliary that occurred with excellent asymmetric induction (>98:2 enantiomeric ratio), a diastereoselective hydroboration/Suzuki-Miyaura coupling reaction sequence, and an atropdiastereoselective biarylcuprate coupling, both of which occurred with total (>20:1) stereocontrol. The syntheses were achieved in six to eight steps from simple aromatic precursors.