135096-78-5 Usage
Uses
Used in Organic Synthesis:
Hydroquinine 9-phenanthryl ether is used as a reagent in organic synthesis for its ability to facilitate the formation of complex organic compounds. Its unique structure allows it to participate in various chemical reactions, making it a valuable component in the synthesis of a wide range of organic products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Hydroquinine 9-phenanthryl ether is used as a precursor in the production of other organic compounds that have medicinal properties. Its potential applications in this field highlight its role in the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
Hydroquinine 9-phenanthryl ether also finds use in the agrochemical industry, where it serves as a starting material for the synthesis of compounds with pesticidal or herbicidal properties. Its contribution to this sector underscores its importance in agricultural chemistry and crop protection.
Used in Material Production:
HYDROQUININE 9-PHENANTHRYL ETHER's unique structure and properties make it suitable for use in the production of various materials. Hydroquinine 9-phenanthryl ether can be incorporated into the manufacturing processes of different materials to enhance their properties or to create new materials with specific characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 135096-78-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,0,9 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 135096-78:
(8*1)+(7*3)+(6*5)+(5*0)+(4*9)+(3*6)+(2*7)+(1*8)=135
135 % 10 = 5
So 135096-78-5 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
135096-78-5Relevant articles and documents
A ligand structure-enantioselectivity relationship for the osmium-catalyzed asymmetric dihydroxylation of olefins
Ogino, Yasukazu,Chen, Hou,Manoury, Eric,Shibata, Tomoyuki,Beller, Matthias,Luebben, Doris,Sharpless, K. Barry
, p. 5761 - 5764 (2007/10/02)
The highest enantioselectivities to date for various olefins are obtained in the osmium-catalyzed asymmetric dihydroxylation using new 9-O-aromatic dihydroquinidine and dihydroquinine ligands. A ligand structure-enantioselectivity relationship (LSER) is developed, and representative results for quinine-based ligands are reported for the first time.