945669-52-3 Usage
Uses
Used in Pharmaceutical Development:
Boc-3-iodotyrosine is utilized as a key component in the synthesis of complex peptides and proteins for the development of new pharmaceuticals. Its role in solid-phase peptide synthesis enables the production of specific peptide sequences that can target various biological pathways and diseases, contributing to the discovery of novel therapeutic agents.
Used in Diagnostics:
In the diagnostics industry, Boc-3-iodotyrosine is employed as a building block for the synthesis of diagnostic peptides and proteins. These synthesized molecules can be used as biomarkers or probes for detecting and monitoring various diseases and conditions, enhancing the accuracy and efficiency of diagnostic tests.
Used in Biotechnology:
Boc-3-iodotyrosine plays a significant role in the biotechnology sector, where it is used as a component in the synthesis of engineered peptides and proteins with specific functions. These molecules can be applied in various biotechnological processes, such as drug delivery, enzyme catalysis, and the development of biosensors.
Used in Research:
In academic and research settings, Boc-3-iodotyrosine is an important tool for studying the structure, function, and interactions of peptides and proteins. Its use in solid-phase peptide synthesis allows researchers to create and investigate specific peptide sequences, providing valuable insights into the underlying mechanisms of biological processes and diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 945669-52-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,6,6 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 945669-52:
(8*9)+(7*4)+(6*5)+(5*6)+(4*6)+(3*9)+(2*5)+(1*2)=223
223 % 10 = 3
So 945669-52-3 is a valid CAS Registry Number.
InChI:InChI=1/C23H29NO5/c1-15-11-18(28-14-17-9-7-6-8-10-17)12-16(2)19(15)13-20(21(25)26)24-22(27)29-23(3,4)5/h6-12,20H,13-14H2,1-5H3,(H,24,27)(H,25,26)/t20-/m0/s1
945669-52-3Relevant articles and documents
Method for Preparing Unnatural Amino Acids
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Paragraph 0165-0168, (2017/01/09)
The present invention relates to a manufacturing method of unnatural amino acids and unnatural amino acids manufactured thereby. Specifically, the present invention relates to an asymmetric synthesis method which can manufacture unnatural amino acids having significantly high optical purity, and to the unnatural amino acids manufactured thereby. A manufacturing method of unnatural amino acids represented by chemical formula 6 or chemical formula 7 comprises the steps of: synthesizing a compound represented by chemical formula 4 or chemical formula 5; manufacturing a diol compound; and manufacturing a carboxylic acid compound.COPYRIGHT KIPO 2016
N-terminally substituted dipeptide amides
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, (2008/06/13)
This invention encompasses compounds of the formula STR1 and the pharmaceutically acceptable acid addition salts thereof wherein R1 is lower alkoxy or --O--(CH2)n -phenyl where the phenyl may be optionally substituted with halogen, --NO2, --CN, --NH2 or lower alkyl wherein n is 1 to 4; R2 and R3 represent lower alkyl, halogen, lower alkoxy or one of R2 or R3 is hydrogen and the other is lower alkyl, lower alkoxy, or halogen; R4, R5, R7, R8, and R9 represent hydrogen or lower alkyl, R6 represents hydrogen, lower alkyl, lower alkenyl, or --(CH2)m -cycloalkyl wherein m is 1 to 4 and the cycloalkyl has 3 to 8 carbon atoms; R10 is --(CH2)p -phenyl wherein p is 1 to 4; and v represents an asymmetric carbon that may be racemic or have the D or L Configuration; w represents an asymmetric carbon when R7 and R8 are not the same that may be racemic or have the D or L configuration. This invention also encompasses compounds where R1 is hydroxy, provided at least one of R4, R5, R6 or R9 is lower alkyl. The compounds of this invention are useful analgesic agents.
