6169-33-1 Usage
Uses
Used in Organic Synthesis:
L-Serine, N-[(phenylmethoxy)carbonyl]-, (4-nitrophenyl)methyl ester is used as a building block in organic synthesis for creating more complex molecules due to its reactivity and ability to undergo various chemical reactions.
Used in Chemical Research:
L-Serine, N-[(phenylmethoxy)carbonyl]-, (4-nitrophenyl)methyl ester is used as a versatile tool in chemical research for studying and developing new compounds and reactions.
Used in Pharmaceutical Development:
L-Serine, N-[(phenylmethoxy)carbonyl]-, (4-nitrophenyl)methyl ester is used as a component in the development of pharmaceutical compounds, particularly due to its (4-nitrophenyl)methyl ester structure, which is useful in the modification of proteins and peptides.
Used in Agrochemical Development:
L-Serine, N-[(phenylmethoxy)carbonyl]-, (4-nitrophenyl)methyl ester is used in the development of agrochemical compounds, where its reactivity and chemical properties can contribute to the creation of new products.
Used in Drug Discovery:
L-Serine, N-[(phenylmethoxy)carbonyl]-, (4-nitrophenyl)methyl ester is used in drug discovery for its potential applications in the study and development of new drugs, particularly in the modification of proteins and peptides.
Used in Study of Biological Systems and Processes:
L-Serine, N-[(phenylmethoxy)carbonyl]-, (4-nitrophenyl)methyl ester is used in the study of biological systems and processes, where its chemical properties can provide insights into the mechanisms and interactions of various biological molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 6169-33-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,6 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6169-33:
(6*6)+(5*1)+(4*6)+(3*9)+(2*3)+(1*3)=101
101 % 10 = 1
So 6169-33-1 is a valid CAS Registry Number.
6169-33-1Relevant academic research and scientific papers
Broadening of the substrate tolerance of α-chymotrypsin by using the carbamoylmethyl ester as an acyl donor in kinetically controlled peptide synthesis
Miyazawa, Toshifumi,Tanaka, Kayoko,Ensatsu, Eiichi,Yanagihara, Ryoji,Yamada, Takashi
, p. 87 - 93 (2007/10/03)
In the kinetically controlled approach of peptide synthesis mediated by α-chymotrypsin, the broadening of the protease's substrate tolerance is achieved by switching the acyl donor from the conventional methyl ester to the carbamoylmethyl ester. Thus, as a typical example, the extremely low coupling efficiency obtained by employing the methyl ester of an inherently poor amino acid substrate, Ala, is significantly improved by the use of this particular ester. Its ameliorating effect is observed also in the couplings of other amino acid residues such as Gly and Ser as carboxy components.
Synthesis of Casein-Related Peptides on Phosphopeptides. VIII. The Synthesis of Ser(P)-Containing Peptides by Use of Z-Ser(PO3R2)-OH Derivatives
Perich, John W.,Alewood, Paul F.,Johns, R. B.
, p. 253 - 263 (2007/10/02)
The synthesis of five Z-Ser(PO3R2)-OH (R = phenyl, ethyl, methyl, benzyl, t-butyl) derivatives is described by a simple three-step synthetic procedure which features the use of ether (A) diphenyl or dialkyl phosphorochloridate/pyridine or (B) dialkyl N,N-
