Fmoc-L-Amino Acids ,  Fmoc-D-Amino Acids,  Fmoc-OPfp Amino Acids,  Boc-L-Amino Acids,  Boc-D-Amino Acids,  Z-Amino Acids,  Unusual Amino Acids,  Amino Acid Derivatives,  N-Methyl Amino Acids,  Amino Acid Alcohols,  Linkers,  Unsubstituted Resins,  Fmoc-Amino Acid-Wang Resins,  Amino Acid 2-Cl-Trt Resins,  MAP Resins,  Pseudoproline Dipeptides,  Reagents 

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StructureCatalog#
CAS#		ProductFormula
MW		Qty/Price*
ABR107

[68262-71-5]		Boc-Arg(Mts)-OH · CHA

C20H32N4O6S C6H13N

555.7		5g   Add 5g of Boc-Arg(Mts)-OH · CHA to my cart
25g   Add 25g of Boc-Arg(Mts)-OH · CHA to my cart
$ 95
$ 350
ABR103

[2188-18-3]		Boc-Arg(NO2)-OH

C11H21N5O6

319.3		100g   Add 100g of Boc-Arg(NO2)-OH to my cart
500g   Add 500g of Boc-Arg(NO2)-OH to my cart
$ 95
$ 380
ABR115

[200124-22-7]		Boc-Arg(Pbf)-OH

C24H38N4O7S

526.7		25g   Add 25g of Boc-Arg(Pbf)-OH to my cart
100g   Add 100g of Boc-Arg(Pbf)-OH to my cart
$ 125
$ 375
ABR110

[13836-37-8]		Boc-Arg(Tos)-OH

C18H28N4O6S

428.5		25g   Add 25g of Boc-Arg(Tos)-OH to my cart
100g   Add 100g of Boc-Arg(Tos)-OH to my cart
$ 90
$ 285
ABR121

[51219-19-3]		Boc-Arg(Z)2-OH

Boc-Arg(Z)2-OH was developed by Meldal and Kindtler (Meldal M., Kindtler JW. Acta Chem. Scand. B 1986, 40, 235-41). They used it in a solution phase synthesis of Boc-Asp-Asp-Tyr-Arg-Gln-Lys-OMe. It is most useful in applications that require full protec.tion of the arginine sidechain. One ex ample is the preparation of optically active aldehyde from arginine derivatives by reduction of arginine O,N-dimethylhydroxamate (Guichard G, Briand JP, Friede M. Pept. Res. 1993, 6,121-4.) Whereas derivatives such as Boc-Arg(Tos)-OH led mainly to byproducts, Boc-Arg(Z)2-OH produced good yields.		C27H34N4O8

542.58		5g   Add 5g of Boc-Arg(Z)2-OH to my cart
25g   Add 25g of Boc-Arg(Z)2-OH to my cart
$ 90
$ 390
ABR101

[35897-34-8]		Boc-Arg-OH · HCl · H2O

C11H22N4O4 HCl H2O

328.8		100g   Add 100g of Boc-Arg-OH · HCl · H2O to my cart
500g   Add 500g of Boc-Arg-OH · HCl · H2O to my cart
$ 100
$ 400
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