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3-tert-butoxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)-propionic acid pentafluorophenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

244633-35-0

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244633-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 244633-35-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,4,6,3 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 244633-35:
(8*2)+(7*4)+(6*4)+(5*6)+(4*3)+(3*3)+(2*3)+(1*5)=130
130 % 10 = 0
So 244633-35-0 is a valid CAS Registry Number.

244633-35-0Downstream Products

244633-35-0Relevant academic research and scientific papers

New solid support for the synthesis of 3′-oligonucleotide conjugates through glyoxylic oxime bond formation

Spinelli, Nicolas,Edupuganti, Om Prakash,Defrancq, Eric,Dumy, Pascal

, p. 219 - 222 (2007/10/03)

(Chemical Equation Presented) A novel solid support 1 was synthesized to incorporate glyoxylic aldehyde functionality at the oligonucleotide 3′-terminus. 6-mer and 11-mer oligonucleotide sequences containing 3′-glyoxylic aldehyde functionality were prepar

Synthesis of aryl esters of protected amino acids from aryl sulfonates

Pudhom, Khanitha,Vilaivan, Tirayut

, p. 5939 - 5942 (2007/10/03)

Aryl esters of Boc- and Fmoc-protected amino acids derived from electron-deficient phenols have been prepared in good yields from aryl 4- nitrobenzenesulfonates in the presence of 1-hydroxy-benzotriazole as catalyst.

9-Fluorenylmethyl Pentafluorophenyl Carbonate as a Useful Reagent for the Preparation of N-9-Fluorenylmethyloxycarbonylamino Acids and their Pentafluorophenyl Esters

Schoen, Istvan,Kisfaludy, Lajos

, p. 303 - 305 (2007/10/02)

9-Fluorenylmethyl pentafluorophenyl carbonate is a useful reagent for the efficient, side reaction-free introduction of N-9-fluorenylmethyloxycarbonyl protecting group into amino acids and for the subsequent preparation of their pentafluorophenyl esters.Some new compounds of both types are described.

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