599178-66-2 Usage
General Description
2-ACETAMIDO-3-(4-BIPHENYL)ACRYLIC ACID is a chemical compound that belongs to the acrylaminde class. It is an acrylaminde derivative with a molecular formula C19H15NO3. 2-ACETAMIDO-3-(4-BIPHENYL)ACRYLIC ACID is used for various purposes including as a monomer for the synthesis of polymers and copolymers, as a starting material in the preparation of pharmaceuticals, and as a component in the manufacture of adhesives and coatings. It is also used in research and development laboratories for its unique chemical properties and potential applications. Additionally, this compound has been studied for its potential therapeutic properties and biological activities, making it an interesting compound for further investigation in the fields of medicinal chemistry and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 599178-66-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,9,1,7 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 599178-66:
(8*5)+(7*9)+(6*9)+(5*1)+(4*7)+(3*8)+(2*6)+(1*6)=232
232 % 10 = 2
So 599178-66-2 is a valid CAS Registry Number.
InChI:InChI=1/C17H15NO3/c1-12(19)18-16(17(20)21)11-13-7-9-15(10-8-13)14-5-3-2-4-6-14/h2-11H,1H3,(H,18,19)(H,20,21)/b16-11+
599178-66-2Relevant articles and documents
Preparation method of chiral alpha-amino acid
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Paragraph 0109; 0110; 0111, (2016/10/08)
The invention discloses a preparation method of chiral alpha-amino acid. Initial raw materials comprising aldehyde and N-acryl substituted glycine undergo Erlenmeyer-Plochl cyclization, hydrolysis or alcoholysis, asymmetric catalytic hydrogenation and acid hydrolysis to obtain the chiral alpha-amino acid compound. The method adopting the above synthesis route has the advantages of mild reaction conditions, simple technological operation, safe and stable production, realization of high yield, good chemical purity and good optical purity of the above obtained product, wide application range, and suitableness for industrial production.
PROCESS FOR THE MANUFACTURE OF N-ACYLBIPHENYL ALANINE
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Page/Page column 13, (2010/04/27)
A novel process, novel process steps and novel intermediates useful in the synthesis of pharmaceutically active N-acylbiphenyl alanine compounds, in particular neutral endopeptidase (NEP) inhibitors.
