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N-[5']Adenylyl-phenylalanine methyl ester, also known as phenylalanyl-adenylate or phenylalanyl-AMP, is a chemical compound formed by the linkage of phenylalanine, an amino acid, to adenosine monophosphate (AMP) through an ester bond. N-[5']adenylyl-phenylalanine methyl ester plays a crucial role in the enzymatic synthesis of phenylalanine, a process known as phenylalanine activation. In this reaction, phenylalanyl-tRNA synthetase catalyzes the formation of phenylalanyl-AMP from phenylalanine and ATP, which is then transferred to the appropriate tRNA molecule, facilitating protein synthesis. Phenylalanyl-AMP is an intermediate in this process and is essential for the accurate incorporation of phenylalanine into growing polypeptide chains during translation.

2131-02-4

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2131-02-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2131-02-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,3 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2131-02:
(6*2)+(5*1)+(4*3)+(3*1)+(2*0)+(1*2)=34
34 % 10 = 4
So 2131-02-4 is a valid CAS Registry Number.

2131-02-4Downstream Products

2131-02-4Relevant academic research and scientific papers

Convenient and regioselective synthesis of nucleoside phosphoramidate monoesters

Zhu, Jigang,Fu, Hua,Jiang, Yuyang,Zhao, Yufen

, p. 1927 - 1929 (2007/10/03)

We have developed a convenient and efficient method for the synthesis of nucleoside phosphoramidate monoesters. This step-wise synthesis, consisting of an ester exchange, reaction of the 5′-OH of nucleosides with fluorenylmethyl aryl phosphite, and an Ath

Reaction of ADP with amino acid methyl esters mediated by trimethylsilyl chloride.

Fu, Hua,Han,Zhao, Yu-Fen

, p. 134 - 135 (2007/10/03)

Reaction of ADP with amino acid methyl esters mediated by trimethylsilyl chloride in pyridine produced adenosine 5'-phosphoramidates in good yields under mild conditions, it is interesting that nucleophilic attack of amino acid methyl esters only occurred

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