135042-88-5 Usage
Description
HYDROQUINIDINE 9-PHENANTHRYL ETHER is a chemical compound that serves as a reagent in various chemical reactions and synthesis processes. It is known for its ability to facilitate the creation of specific compounds, such as antifungal indole alkaloids, N-reverse prenylated tryptophan, and deoxy sugar.
Uses
Used in Pharmaceutical Industry:
HYDROQUINIDINE 9-PHENANTHRYL ETHER is used as a reagent for the synthesis of antifungal indole alkaloids and N-reverse prenylated tryptophan. These compounds are essential in the development of new drugs and therapies to combat various fungal infections and other medical conditions.
Used in Chemical Synthesis:
HYDROQUINIDINE 9-PHENANTHRYL ETHER is used as a reagent for the synthesis of deoxy sugar via Wharton rearrangement and stereoselective dihydroxylation reaction. These processes are crucial in the production of complex organic compounds and contribute to the advancement of chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 135042-88-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,0,4 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 135042-88:
(8*1)+(7*3)+(6*5)+(5*0)+(4*4)+(3*2)+(2*8)+(1*8)=105
105 % 10 = 5
So 135042-88-5 is a valid CAS Registry Number.
InChI:InChI=1/C34H34N2O2/c1-3-22-21-36-17-15-23(22)19-32(36)34(29-14-16-35-31-13-12-26(37-2)20-30(29)31)38-33-27-10-6-4-8-24(27)18-25-9-5-7-11-28(25)33/h4-14,16,18,20,22-23,32,34H,3,15,17,19,21H2,1-2H3/t22-,23?,32?,34+/m1/s1
135042-88-5Relevant articles and documents
Syntheses and crystal structures of the cinchona alkaloid derivatives used as ligands in the osmium-catalyzed asymmetric dihydroxylation of olefins
Amberg,Bennani,Chadha,Crispino,Davis,Hartung,Jeong,Ogino,Shibata,Sharpless
, p. 844 - 849 (1993)
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New Ligands Double the Scope of the Catalytic Asymmetric Dihydroxylation of Olefins
Sharpless, K. Barry,Amberg, Willi,Beller, Matthias,Chen, Hou,Hartung, Jens,et al.
, p. 4585 - 4588 (2007/10/02)
Improved ligands render terminal olefins good substrates for the osmium-catalyzed asymmetric dihydroxylation (ADH) process, and the amounts of chiral ligand and osmium catalyst required diminish dramatically.
