5068-29-1 Usage
General Description
Z-TYR(TBU)-OME, also known as Benzyloxycarbonyl-O-tert-butyl-L-tyrosine methyl ester, is a specific type of organic compound that belongs to the class of chemical entities known as Phenylpropanoic acids. These are compounds with a structure containing a benzene ring conjugated to a propanoic acid. This chemical is often used in various biological and chemical research, including the synthesis of peptides for pharmaceutical applications. Its chemical formula is C19H23NO5 and it is soluble with a molecular weight of approximately 347.4 g/mol. As a protected form of the amino acid tyrosine, it is primarily used in the process of peptide synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 5068-29-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,6 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5068-29:
(6*5)+(5*0)+(4*6)+(3*8)+(2*2)+(1*9)=91
91 % 10 = 1
So 5068-29-1 is a valid CAS Registry Number.
5068-29-1Relevant articles and documents
Syntheses of amino alcohols and chiral C2-symmetric bisoxazolines derived from O-alkylated R-4-hydroxyphenylglycine and S-tyrosine
Caplar, Vesna,Raza, Zlata,Katalenic, Darinka,Zinic, Mladen
, p. 23 - 36 (2007/10/03)
Chiral C2-symmetric bisoxazolines 1b-f and 2b,c, derived from 4′-O-alkylated R-4-hydroxyphenylglycine or S-tyrosine, were prepared. As intermediates, a series of chiral amino alcohols possessing substituted phenolic groups was prepared and fully characterized.
Total synthesis of cyclotheonamide B, a facile route towards analogues
Bastiaans, Harold M. M.,Van Der Baan, Juul L.,Ottenheijm, Harry C. J.
, p. 5963 - 5966 (2007/10/02)
A flexible, convergent synthesis of cyclotheonamide B (1b) was developed, starting from the constituent amino acids, using conventional benzyl-, t-butyl- and allyl-based protecting groups. By modification of the key intermediates, this approach allows the preparation of cyclotheonamide analogues.
