81115-66-4 Usage
Uses
Used in Pharmaceutical Industry:
(S)-(-)-2-phenylpropyl (R)-(-)-2-phenylpropanoate is used as an intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its unique structure allows for the creation of novel drugs with specific therapeutic properties.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-(-)-2-phenylpropyl (R)-(-)-2-phenylpropanoate serves as a key building block for the development of complex organic molecules. It is used as a [application type] for [application reason], such as constructing specific molecular frameworks or functional groups that are difficult to access through traditional synthetic routes.
Used in Chemical Production Processes:
(S)-(-)-2-phenylpropyl (R)-(-)-2-phenylpropanoate is also utilized in chemical production processes as a [application type] for [application reason]. Its unique reactivity and structural features make it a valuable component in the manufacturing of specialty chemicals, fine chemicals, or other advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 81115-66-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,1,1 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 81115-66:
(7*8)+(6*1)+(5*1)+(4*1)+(3*5)+(2*6)+(1*6)=104
104 % 10 = 4
So 81115-66-4 is a valid CAS Registry Number.
81115-66-4Relevant academic research and scientific papers
Asymmetric Reaction of (RS)-2-Phenylpropanal with Chiral Aluminium Alkoxides. Part 1
Maslinska-Solich, Jolanta,Rudnicka, Irena,Jedlinski, Zbigniew J.
, p. 3034 - 3040 (2007/10/02)
The reaction of chiral aluminium alkoxides (2) with (RS)-2-phenylpropanal (1) gives the optically active (S)-(-)-2-phenylpropyl (R)-(-)-2-phenylpropanoate (3), and the mixed esters (-)-menthyl 2-phenylpropanoate (5a), (+)-2-phenylpropyl 2-methylbutanoate (4b), and (+)-2-methylbutyl 2-phenylpropanoate (5b), respectively.An asymmetric disproportionation reaction mechanism has been proposed for compound (1).
