63126-52-3 Usage
Uses
Used in Chemical Synthesis:
(S,S)-(-)-2,3-DIHYDROXY-N,N,N',N'-TETRAMETHYLSUCCINAMIDE is used as an intermediate in the synthesis of Diethyl D-(-)-Tartrate, which is a chiral reagent in a variety of chemical reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (S,S)-(-)-2,3-DIHYDROXY-N,N,N',N'-TETRAMETHYLSUCCINAMIDE is used as a chiral reagent for the synthesis of various drugs, including marin toxin and antitumor agent phorboxazole A.
Used in Asymmetric Syntheses:
(S,S)-(-)-2,3-DIHYDROXY-N,N,N',N'-TETRAMETHYLSUCCINAMIDE is also used in asymmetric syntheses of S,S-dialkyl-substituted sulfoximines, which are important compounds in the development of new pharmaceuticals and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 63126-52-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,2 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 63126-52:
(7*6)+(6*3)+(5*1)+(4*2)+(3*6)+(2*5)+(1*2)=103
103 % 10 = 3
So 63126-52-3 is a valid CAS Registry Number.
63126-52-3Relevant academic research and scientific papers
From single molecule to crystal: Mapping out the conformations of tartaric acids and their derivatives
Janiak, Agnieszka,Rychlewska, Urszula,Kwit, Marcin,Stepien, Urszula,Gawronska, Krystyna,Gawronski, Jacek
experimental part, p. 1500 - 1506 (2012/07/28)
Stereoisomers of one of the most important organic compounds, tartaric acid, optically active and meso as well as the ester or amide derivatives, can show diverse structures related to the rotation around the three carbon-carbon bonds. This study determin
PENTACO-ORDINATE ORGANOSILICON COMPOUNDS IN SYNTHESIS: ASYMMETRIC REDUCTION OF CARBONYL COMPOUNDS WITH HYDROSILANES CATALYZED BY CHIRAL BASES
Kohra, Shinya,Hayashida, Hisashi,Tominaga, Yoshinori,Hosomi, Akira
, p. 89 - 92 (2007/10/02)
Reduction of carbonyl compounds with trialkoxysilane can be readily catalyzed by alkoxides of alkali metal.A considerable high asymmetric induction takes place by use of optically active diolates or even N-lithio 2-amino alcoholates derived from optically
