50833-50-6 Usage
Description
(S)-2-Benzyloxycarbonylamino-heptanoic acid, with the chemical formula C16H21NO4, is an amino acid derivative featuring a benzyl group and a carbonyl group attached to the alpha carbon. (S)-2-Benzyloxycarbonylamino-heptanoic acid is significant in the field of organic chemistry due to its protective role for the amino group and its facilitation of reactions at the alpha carbon, making it instrumental in the synthesis of complex molecular structures.
Uses
Used in Organic Chemistry:
(S)-2-Benzyloxycarbonylamino-heptanoic acid is used as a building block for the synthesis of various peptides and proteins. Its unique structure allows for the protection of the amino group and facilitates reactions at the alpha carbon, making it a valuable tool in the creation of complex molecular structures.
Used in Pharmaceutical Development:
(S)-2-Benzyloxycarbonylamino-heptanoic acid is used as a precursor in the development of pharmaceuticals and biologically active compounds. Its potential applications in this field make it a promising target for further research and development, with the aim of discovering new therapeutic agents and treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 50833-50-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,8,3 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 50833-50:
(7*5)+(6*0)+(5*8)+(4*3)+(3*3)+(2*5)+(1*0)=106
106 % 10 = 6
So 50833-50-6 is a valid CAS Registry Number.
50833-50-6Relevant articles and documents
Optical Resolution of Unusual Amino-Acids by Lipase-catalysed Hydrolysis
Miyazawa, Toshifumi,Takitani, Tadanori,Ueji, Shinichi,Yamada, Takashi,Kuwata, Shigeru
, p. 1214 - 1216 (1988)
The 2-chloroethyl esters of the N-benzyloxycarbonyl (Z) derivatives of several unusual amino-acids are converted by Aspergillus niger lipase into enantiomerically enriched Z-amino-acids with fairly high optical purities, the L-enantiomers being preferentially hydrolysed.
