1345628-08-1 Usage
Uses
Used in Pharmaceutical Applications:
(11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-di-9-anthracenyl-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-oxide is used as a potential drug candidate due to its unique chemical structure and properties. It may have therapeutic effects in various medical conditions, although further research is needed to explore its full potential.
Used in Organic Chemistry Research:
(11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-di-9-anthracenyl-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-oxide is used as a building block for the synthesis of other complex organic compounds. Its unique structure makes it an interesting subject for further research and exploration in the field of organic chemistry, potentially leading to the development of new compounds with various applications.
Used in Chemical Industry:
(11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-di-9-anthracenyl-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-oxide may also find use in the chemical industry for various purposes, such as in the development of new materials, catalysts, or other chemical processes. Its specific properties and structure could contribute to innovative solutions in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 1345628-08-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,5,6,2 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1345628-08:
(9*1)+(8*3)+(7*4)+(6*5)+(5*6)+(4*2)+(3*8)+(2*0)+(1*8)=161
161 % 10 = 1
So 1345628-08-1 is a valid CAS Registry Number.
1345628-08-1Relevant articles and documents
The catalytic asymmetric Fischer indolization
Mueller, Steffen,Webber, Matthew J.,List, Benjamin
, p. 18534 - 18537 (2012/01/31)
The first catalytic asymmetric Fischer indolization is reported. In the presence of a 5 mol % loading of a novel spirocyclic chiral phosphoric acid, 4-substituted cyclohexanone-derived phenylhydrazones undergo a highly enantioselective indolization. Efficient catalyst turnover was achieved by the addition of a weakly acidic cation exchange resin, which removes the generated ammonia. The reaction can be conducted under mild conditions and gives various 3-substituted tetrahydrocarbazoles in generally high yields.