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Code Name Synonym
FM-186 Fmoc-Abu(3-Alloc-amino) (2R,3R) 2-(Fmoc-amino)-3-(Alloc-amino)butanoic acid
CAS 1263047-57-9 /upload/more_svg/small/small_fm-186.svg
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 /upload/more_svg/small/small_FM-196.svg
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 /upload/more_svg/small/small_FM-184.svg
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 /upload/more_svg/small/small_ET-068.svg
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 /upload/more_svg/small/small_FM-193.svg
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 /upload/more_svg/small/small_FM-192.svg
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 /upload/more_svg/small/small_dd-188.svg
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 /upload/more_svg/small/small_dd-187.svg
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 /upload/more_svg/small/small_DD-010.svg
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 /upload/more_svg/small/small_DD-049.svg
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

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