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N-Fmoc-[18O2]phenylalanine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1005482-88-1

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1005482-88-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1005482-88-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,5,4,8 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1005482-88:
(9*1)+(8*0)+(7*0)+(6*5)+(5*4)+(4*8)+(3*2)+(2*8)+(1*8)=121
121 % 10 = 1
So 1005482-88-1 is a valid CAS Registry Number.

1005482-88-1Downstream Products

1005482-88-1Relevant academic research and scientific papers

Microwave-assisted 18O labeling of Fmoc-protected amino acids

Modzel, Maciej,Plciennik, Halina,Kluczyk, Alicja,Stefanowicz, Piotr,Szewczuk, Zbigniew

, p. 896 - 900 (2014)

Recently, there has been an increased interest in isotopical labeling of peptides. Although there are several techniques allowing for a complete labeling of all carboxyl groups in peptides, regioselective labeling would be beneficial in many situations. Such labeling requires the use of 18O-labeled Fmoc amino acids. We have designed a method for such labeling that is an improvement on a technique proposed earlier. The new procedure is suitable for microscale synthesis and could be used in peptide and proteomics laboratories. Although for the majority of tested amino acids our method gives good labeling efficiency, it is time consuming. Therefore, we have decided to use microwave-assisted procedure. This approach resulted in reduction of reaction time to 15 min and increased reaction efficiency.

Microwave-assisted 18O labeling of Fmoc-protected amino acids

Modzel, Maciej,P?óciennik, Halina,Kluczyk, Alicja,Stefanowicz, Piotr,Szewczuk, Zbigniew

, p. 896 - 900 (2015/02/19)

Recently, there has been an increased interest in isotopical labeling of peptides. Although there are several techniques allowing for a complete labeling of all carboxyl groups in peptides, regioselective labeling would be beneficial in many situations. Such labeling requires the use of 18O-labeled Fmoc amino acids. We have designed a method for such labeling that is an improvement on a technique proposed earlier. The new procedure is suitable for microscale synthesis and could be used in peptide and proteomics laboratories. Although for the majority of tested amino acids our method gives good labeling efficiency, it is time consuming. Therefore, we have decided to use microwave-assisted procedure. This approach resulted in reduction of reaction time to 15 min and increased reaction efficiency.

HIV-1 PROTEASE TRANSITION STATE AND USES THEREOF

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Paragraph 0034, (2013/09/12)

Methods and systems for obtaining inhibitors of human immunodeficiency virus- 1 (HIV-1) protease are disclosed where the methods involve designing compounds that resemble the HIV-1 protease transition state.

Synthesis of isotopically labeled P-site substrates for the ribosomal peptidyl transferase reaction

Zhong, Minghong,Strobel, Scott A.

, p. 603 - 611 (2008/09/17)

(Chemical Equation Presented) Isotopomers of the ribosomal P-site substrate, the trinucleotide peptide conjugate CCA-pcb (Zhong, M.; Strobel, S. A. Org. Lett. 2006, 8, 55-58), have been designed and synthesized in 26-35 steps. These include individual iso

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