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(3R,5R)-5-benzyloxy-3-hydroxyhexanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

115407-98-2

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115407-98-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115407-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,4,0 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 115407-98:
(8*1)+(7*1)+(6*5)+(5*4)+(4*0)+(3*7)+(2*9)+(1*8)=112
112 % 10 = 2
So 115407-98-2 is a valid CAS Registry Number.

115407-98-2Downstream Products

115407-98-2Relevant academic research and scientific papers

Reagent-Controlled Addition of (R)- and (S)-2-Hydroxy-1,2,2-triphenylethyl Acetate to Chiral Aldehydes

Mahler, Ulrike,Devant, Ralf M.,Braun, Manfred

, p. 2035 - 2044 (2007/10/02)

The enantiomeric enolates (R)- and (S)-2, generated by double deprotonation of (R)- and (S)-2-hydroxy-1,2,2-triphenylethyl acetate (1) ("HYTRA"), are added to chiral aldehydes 4.It turnes out, that in this aldol reaction, the stereochemistry is largely determined by the configuration of the enolate 2 ("reagent control").Depending on the enantiomer of the reagent 1, which is combined with one of the enantiomerically pure aldehydes 4, either anti or syn adducts 11 and 12 are formed predominantly.The basic hydrolysis of the crude adducts 11/12 affords anti and syn carboxylic acids 5 and 6 in the corresponding diastereomeric ratios.By recrystallization of some of the mixtures 11/12, the esters 11c, 11e, and 11g are available in high diastereomeric and enantiomeric purity.Scope and limitations of the method are discussed.

Stereoselektive Aldolreaktionen mit α-unsubstituierten chiralen Enolaten

Braun, Manfred

, p. 24 - 37 (2007/10/02)

Die Aldolreaktion gehoert zu den wichtigsten CC-Verknuepfungsmethoden.Mit der Addition eines Enolats an einen Aldehyd geht die Entstehung mindestens eines Chiralitaetszentrums einher.Waehrend die Kontrolle der Stereochemie im Falle α-unsubstituierter Enolate weitgehend erreicht werden konnte, war die Aldolreaktion α-substituierter chiraler Enolate wegen unzureichender Stereoselektivitaet lange Zeit ein "Sorgenkind" der Synthetiker.Fortschritte auf diesem Gebiet konnten erst in den letzten Jahren erzielt werden, und zwar mit neuen chiralen Hilfsgruppen sowie mit Alternativen zur Aldolreaktion.

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