Code |
Name |
Synonym |
FM-186 |
Fmoc-Abu(3-Alloc-amino) (2R,3R) |
2-(Fmoc-amino)-3-(Alloc-amino)butanoic acid |
CAS |
1263047-57-9 |
 |
Formula |
C23H24N2O6 |
MW |
424.4 |
Purity |
>98% |
Storage |
+2 ... +8 °C |
Code |
Name |
Synonym |
FM-196 |
Fmoc-Abu(3-Alloc-amino) (2S,3R) |
2-(Fmoc-amino)-3-(Alloc-amino)butanoic acid (2S,3R) |
CAS |
|
 |
Formula |
C23H24N2O6 |
MW |
424.4 |
Purity |
>98% |
Storage |
+2 ... +8 °C |
Code |
Name |
Synonym |
FM-184 |
Fmoc-Abu(3-Alloc-amino) (2S,3S) |
2-(Fmoc-amino)-3-(Alloc-amino)butanoic acid |
CAS |
1272754-91-2 |
 |
Formula |
C23H24N2O6 |
MW |
424.4 |
Purity |
>98% |
Storage |
+2 ... +8 °C |
Note |
Used as an orthogonally protected building-block in solid-phase peptide synthesis. |
Code |
Name |
Synonym |
ET-068 |
Alloc-AEEA.DCHA |
[2-[2-(Alloc-amino)ethoxy]ethoxy]acetic acid.DCHA // Alloc-8-amino-3,6-dioxaoctanoic acid.DCHA // Aloc-AEEA.DCHA // Alloc-O2Oc.DCHA // Alloc-Ado.DCHA // Aloc-Adoa.DCHA |
CAS |
560088-74-6 , 431990-38-4 net |
 |
Formula |
C22H40N2O6 |
MW |
428.6 |
Purity |
>99% |
Storage |
+2 ... +8 °C |
Code |
Name |
Synonym |
FM-193 |
Fmoc-Pro(4-NH-Alloc) (2S,4R) |
(4R)-4-Allyloxycarbonylamino-1-(9-fluorenylmethyloxycarbonyl)-L-proline // Fmoc-Pro(4-NH-Alloc)-OH (2S,4R) |
CAS |
273222-05-2 |
 |
Formula |
C24H24N2O6 |
MW |
436.5 |
Purity |
>98% |
Storage |
+2 ... +8 °C |
Note |
Fmoc-Pro(4-NH-Alloc) is an orthogonally protected building block used in peptide synthesis. J. Med. Chem. (2009), 52(21), 6744-6751. DOI:10.1021/jm9012032. |
Code |
Name |
Synonym |
FM-192 |
Fmoc-Pro(4-NH-Alloc) (2S,4S) |
(4S)-4-Allyloxycarbonylamino-1-(9-fluorenylmethyloxycarbonyl)-L-proline // Fmoc-Pro(4-NH-Alloc)-OH (2S,4S) |
CAS |
274676-10-7 |
 |
Formula |
C24H24N2O6 |
MW |
436.5 |
Purity |
>98% |
Storage |
+2 ... +8 °C |
Note |
Fmoc-Pro(4-NH-Alloc) is used in peptide synthesis. Chemical Communications (2016), 52(59), 9275-9278. DOI:10.1039/C6CC04672J; Tetrahedron (2012), 68(23), 4406-4412. DOI:10.1016/j.tet.2012.02.003. |
Code |
Name |
Synonym |
DD-188 |
Alloc-Dab(Fmoc) |
Aloc-Dab(Fmoc) // Alloc-L-Dab(Fmoc) // N-alpha-Alloc-N-gamma-Fmoc-L-2,4-diaminobutyric acid |
CAS |
460751-78-4 |
 |
Formula |
C23H24N2O6 |
MW |
424.5 |
Purity |
>98% |
Storage |
+2 ... +8 °C |
Code |
Name |
Synonym |
DD-187 |
Alloc-Dap(Fmoc) |
Aloc-Dap(Fmoc) // Alloc-L-Dap(Fmoc) // N-alpha-Alloc-N-beta-Fmoc-L-2,4-diaminopropionic acid |
CAS |
176755-00-3 |
 |
Formula |
C22H22N2O6 |
MW |
410.4 |
Purity |
>98% |
Storage |
+2 ... +8 °C |
Code |
Name |
Synonym |
DD-010 |
Boc-Dap(Alloc) |
N-alpha-Boc-N-beta-Alloc-L-2,3-diaminopropionic acid // Boc-Dap(Aloc)-OH // Boc-Dpr(Aloc)-OH // Boc-Dapa(Aloc)-OH |
CAS |
161561-83-7 |
 |
Formula |
C12H20N2O6 |
MW |
288.3 |
Purity |
>98% |
Storage |
+2 ... +8 °C |
Specification |
Link |
Code |
Name |
Synonym |
DD-049 |
Fmoc-Dap(Alloc) |
N-alpha-Fmoc-N-beta-Alloc-L-2,3-diaminopropionic acid // Fmoc-Dap(Aloc)-OH // Fmoc-Dpr(Aloc)-OH // Fmoc-Dapa(Aloc)-OH |
CAS |
188970-92-5 |
 |
Formula |
C22H22N2O6 |
MW |
410.4 |
Purity |
>99% |
Enantiopurity |
>99.9% |
Storage |
+2 ... +8 °C |
Note |
Fmoc-Dap(Alloc) is used in peptide synthesis where orthogonal to Fmoc- and Boc- side-chain protecting group is needed. DOI:10.1021/JA9642121; DOI:10.1021/ja804754y; Science (2010), 330(6011), 1689-1692. DOI:10.1126/science.1196154; DOI:10.1002/anie.200906620; Nature Chemistry (2018), 10(7), 704-714. DOI:10.1038/s41557-018-0033-8. |
Specification |
Link |