70094-90-5 Usage
Uses
Used in Pharmaceutical Industry:
(S)-(-)-3-(4-chlorophenyl)-3-hydroxypropionic acid is used as an active pharmaceutical ingredient for its ability to inhibit the growth of bacteria and fungi. Its antimicrobial properties make it a valuable component in the development of medications targeting various infections.
Used in Agrochemical Industry:
In the agrochemical industry, (S)-(-)-3-(4-chlorophenyl)-3-hydroxypropionic acid is used as a component in the development of fungicides and bactericides to protect crops from diseases caused by microbial pathogens.
Used in Chiral Drug Preparation:
(S)-(-)-3-(4-chlorophenyl)-3-hydroxypropionic acid is used as a key intermediate in the synthesis of chiral drugs. Its chiral center allows for the creation of enantiomer-specific medications, which can have different effects and potencies in the body.
Used as a Precursor in Chemical Synthesis:
(S)-(-)-3-(4-chlorophenyl)-3-hydroxypropionic acid serves as a precursor in the synthesis of various important chemicals, including those used in the production of specialty materials and other high-value compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 70094-90-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,0,9 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70094-90:
(7*7)+(6*0)+(5*0)+(4*9)+(3*4)+(2*9)+(1*0)=115
115 % 10 = 5
So 70094-90-5 is a valid CAS Registry Number.
70094-90-5Relevant academic research and scientific papers
Asymmetric synthesis of both antipodes of β-hydroxy nitriles and β-Hydroxy carboxylic acids via enzymatic reduction or sequential reduction/hydrolysis
Ankati, Haribabu,Zhu, Dunming,Yang, Yan,Biehl, Edward R.,Hua, Ling
supporting information; experimental part, p. 1658 - 1662 (2009/08/08)
Use of isolated carbonyl reductases in the reduction of aromatic β-ketonitriles have completely eliminated the competing α-ethylation, which is often observed with whole cell biocatalysts. By choosing suitable recombinant carbonyl reductase, the reduction
New chiral acetate imide enolate for stereoselective aldol reactions
Palomo, Claudio,Oiarbide, Mikel,Gonzalez, Alberto,Garcia, Jesus M.,Berree, Fabienne,Linden, Anthony
, p. 6931 - 6934 (2007/10/03)
The chiral imide acetate 4 reacts upon lithium and titanium enolate formation conditions with aldehydes in a stereoselective manner. Remarkably, aldols obtained from aromatic and α,β-unsaturated aldehydes exhibited opposite stereochemistry than those obtained from aliphatic aldehydes.
