218608-77-6 Usage
General Description
"(R)-3-(p-Benzyloxyphehnyl)-beta-alanine" is a chemical compound that belongs to the class of beta-alanine derivatives. It is a white solid with a molecular formula C17H18N2O3 and a molecular weight of 298.34 g/mol. (R)-3-(P-BENZYLOXYPHENYL)-BETA-ALANINE is often used in pharmaceutical research and drug development due to its potential therapeutic applications, including its ability to act as a GABAB receptor agonist and its potential antianxiety and anticonvulsant properties. Its p-benzyloxyphenyl group provides structural features that are important for its biological activity, making it a promising candidate for further investigation in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 218608-77-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,8,6,0 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 218608-77:
(8*2)+(7*1)+(6*8)+(5*6)+(4*0)+(3*8)+(2*7)+(1*7)=146
146 % 10 = 6
So 218608-77-6 is a valid CAS Registry Number.
InChI:InChI=1/C16H17NO3/c17-15(10-16(18)19)13-6-8-14(9-7-13)20-11-12-4-2-1-3-5-12/h1-9,15H,10-11,17H2,(H,18,19)/t15-/m1/s1
218608-77-6Relevant articles and documents
Novel efficient method for synthesizing chiral beta-amino acid
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Paragraph 0047; 0049; 0051; 0061; 0062; 0063, (2019/01/08)
The invention relates to a synthesis method of a compound as shown by the formula (I), namely chiral beta-amino acid: an aromatic aldehyde compound. An aromatic aldehyde compound and a chiral amine auxiliary form Schiff base, and then the Schiff base is r
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.
