865812-10-8 Usage
Description
(R)-O-TOLYL-CBS-OXAZABOROLIDINE, 0.5M I& is a chiral catalyst that plays a crucial role in various organic reactions. It is specifically designed to facilitate enantioselective processes, ensuring that the desired chiral products are formed with high selectivity and purity.
Uses
Used in Pharmaceutical Industry:
(R)-O-TOLYL-CBS-OXAZABOROLIDINE, 0.5M I& is used as a chiral catalyst for enantioselective Diels-Alder reactions, which are essential in the synthesis of complex organic molecules, particularly in the development of pharmaceutical compounds. The high selectivity provided by this catalyst ensures that the desired enantiomer is produced, leading to more effective and safer drugs.
Used in Chemical Research:
In the field of chemical research, (R)-O-TOLYL-CBS-OXAZABOROLIDINE, 0.5M I& is employed as a chiral catalyst to study and develop new enantioselective reactions. This allows researchers to explore the potential of these reactions in creating novel chiral compounds with unique properties and applications.
Used in Fine Chemicals Industry:
(R)-O-TOLYL-CBS-OXAZABOROLIDINE, 0.5M I& is utilized as a chiral catalyst in the production of fine chemicals, which are high-purity specialty chemicals used in various applications such as fragrances, flavors, and agrochemicals. The enantioselective capabilities of this catalyst ensure that the desired chiral products are synthesized with high purity, enhancing the performance and quality of the final products.
Check Digit Verification of cas no
The CAS Registry Mumber 865812-10-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,5,8,1 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 865812-10:
(8*8)+(7*6)+(6*5)+(5*8)+(4*1)+(3*2)+(2*1)+(1*0)=188
188 % 10 = 8
So 865812-10-8 is a valid CAS Registry Number.
InChI:InChI=1/C24H24BNO/c1-19-11-8-9-16-22(19)25-26-18-10-17-23(26)24(27-25,20-12-4-2-5-13-20)21-14-6-3-7-15-21/h2-9,11-16,23H,10,17-18H2,1H3/t23-/m1/s1
865812-10-8Relevant articles and documents
Enantioselective Strecker and Allylation Reactions with Aldimines Catalyzed by Chiral Oxazaborolidinium Ions
Kang, Ki-Tae,Park, Sang Hyun,Ryu, Do Hyun
supporting information, p. 6679 - 6683 (2019/09/12)
Chiral oxazaborolidinium ion (COBI)-catalyzed enantioselective nucleophilic addition reactions of aldimines using tributyltin cyanide and allyltributylstannane have been developed. Various α-aminonitriles and homoallylic amines were synthesized in high yi
HIV-1 PROTEASE INHIBITORS AND USES THEREOF
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, (2016/04/26)
Various embodiments of the present invention are directed to compounds of the formula (I) or a pharmaceutically acceptable salt, polymorph, prodrug, solvate or clathrate thereof, wherein X1, X2, X3, R1, R2, R11, and n are defined herein. These compounds are useful as inhibitors of HIV-1 protease and, as a result, are useful in the treatment of HIV infection.
SOLID FORMS OF 2-(TERT-BUTYLAMINO)-4-((1R,3R,4R)-3-HYDROXY-4-METHYLCYCLOHEXYLAMINO)-PYRIMIDINE-5-CARBOXAMIDE, COMPOSITIONS THEREOF AND METHODS OF THEIR USE
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Paragraph 00453, (2015/11/02)
Provided herein are formulations, processes, solid forms and methods of use relating to 2- (tert-butylamino)-4-((lR,3R,4R)-3-hydroxy-4-methylcyclohexylamino)-pyrimidine-5- carboxamide.
