752198-18-8 Usage
Uses
Used in Pharmaceutical Development:
(S)-3-AMINO-3-(2,3-DIMETHOXY-PHENYL)-PROPIONIC ACID is used as a building block in the synthesis of new pharmaceuticals due to its complex structure and reactivity. Its combination of functional groups and chiral center may offer unique opportunities for the creation of innovative drug molecules with specific therapeutic properties.
Used in Material Science:
In the field of material science, (S)-3-AMINO-3-(2,3-DIMETHOXY-PHENYL)-PROPIONIC ACID is used as a precursor for the development of new materials. Its chemical properties, including the potential for interesting reactions due to the phenyl ring and methoxy substituents, could lead to the creation of advanced materials with specialized applications.
Used in Synthetic Chemistry Research:
(S)-3-AMINO-3-(2,3-DIMETHOXY-PHENYL)-PROPIONIC ACID serves as a subject of study in synthetic chemistry research. Its unique structure and properties make it an interesting compound for exploring new synthetic pathways and understanding the effects of chirality on chemical reactions and product outcomes.
Without specific information on the compound's applications or origins, these uses are based on general observations of its structure and potential properties. Further research and development would be necessary to fully realize the compound's practical applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 752198-18-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,2,1,9 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 752198-18:
(8*7)+(7*5)+(6*2)+(5*1)+(4*9)+(3*8)+(2*1)+(1*8)=178
178 % 10 = 8
So 752198-18-8 is a valid CAS Registry Number.
752198-18-8Relevant academic research and scientific papers
Competitive formation of β-amino acids, propenoic, and ylidenemalonic acids by the Rodionov reaction from malonic acid, aldehydes, and ammonium acetate in alcoholic medium
Lebedev,Lebedeva,Sheludyakov,Kovaleva,Ustinova,Kozhevnikov
, p. 1113 - 1124 (2007/10/03)
The Rodionov reaction of 49 available aliphatic and aromatic aldehydes with malonic acid and ammonium acetate in alcoholic medium, resulting in formation of β-amino acids, propenoic, and ylidenemalonic acids, was studied. Certain regioselectivity regularities of the reaction were revealed. Among the variety of ketones studied, cyclohexanone is the only whose reaction yields a β-amino acid. Unusual dehydrofluorination of 6-chloro-2-fluorocinnamic acid under the Rodionov reaction was discovered. 2005 Pleiades Publishing, Inc.
One-Pot Cyclization of Alkoxy-3-Aminoindan-1-ones.
Dallemagne, Patrick,Rault, Sylvain,Pilo, Juan Carlos,Foloppe, Marie Paule,Robba, Max
, p. 6327 - 6328 (2007/10/02)
3-Amino-3-alkoxyphenylpropionic acids, prepared from alkoxybenzaldehydes, are cyclized in one step into 3-aminoindan-1-ones using trifluoroacetic acid and trifluoroacetic anhydride. Key Words: One-pot cyclization; Aminoindanones; Electrodonating substitue
