878011-67-7 Usage
General Description
(S)-3-AMINO-4-(4-METHOXYPHENYL)BUTANOIC ACID, also known as (S)-4-(4-METHOXYPHENYL)-3-AMINOBUTANOIC ACID or (S)-HOMOPHENYLALANINE, is a chemical compound with the molecular formula C11H15NO3. It is a non-proteinogenic amino acid, which means it is not incorporated into proteins during translation. (S)-3-AMINO-4-(4-METHOXYPHENYL)BUTANOIC ACID is often used in the synthesis of peptides and pharmaceuticals, and it has potential applications in the treatment of various medical conditions. It is also a useful tool in the study of biological systems and drug development. (S)-3-AMINO-4-(4-METHOXYPHENYL)BUTANOIC ACID is a chiral molecule, meaning it has two enantiomers, or mirror-image forms, and the (S)-enantiomer is the biologically active form. Overall, (S)-3-AMINO-4-(4-METHOXYPHENYL)BUTANOIC ACID has significant potential for various research and practical applications in the fields of chemistry, pharmaceuticals, and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 878011-67-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,8,0,1 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 878011-67:
(8*8)+(7*7)+(6*8)+(5*0)+(4*1)+(3*1)+(2*6)+(1*7)=187
187 % 10 = 7
So 878011-67-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO3/c1-15-10-4-2-8(3-5-10)6-9(12)7-11(13)14/h2-5,9H,6-7,12H2,1H3,(H,13,14)/t9-/m0/s1
878011-67-7Relevant articles and documents
A novel approach to homochiral β-amino acids 1
Seki, Masahiko,Matsumoto, Kazuo
, p. 3165 - 3168 (2007/10/03)
An efficient synthesis of γ-aryl or alkyl substituted β-amino acids starting from N-Cbz-L-homoserine lactone via the formation of α-amino aryl, alkenyl or alkynyl ketones with the original α-carbon chirality retained as such is described. Copyright