534404
N-Boc-cis-4-N-Fmoc-amino-L-proline
97%
Synonym(s):
(2S,4S)-N-tert-Butoxycarbonyl-4-N-(9-fluorenylmethoxycarbonyl)aminopyrrolidine-2-carboxylic acid
About This Item
Recommended Products
Assay
97%
optical activity
[α]20/D -68°, c = 1 in chloroform
reaction suitability
reaction type: Boc solid-phase peptide synthesis
mp
150-154 °C (lit.)
application(s)
peptide synthesis
functional group
Boc
Fmoc
SMILES string
CC(C)(C)OC(=O)N1C[C@H](C[C@H]1C(O)=O)NC(=O)OCC2c3ccccc3-c4ccccc24
InChI
1S/C25H28N2O6/c1-25(2,3)33-24(31)27-13-15(12-21(27)22(28)29)26-23(30)32-14-20-18-10-6-4-8-16(18)17-9-5-7-11-19(17)20/h4-11,15,20-21H,12-14H2,1-3H3,(H,26,30)(H,28,29)/t15-,21-/m0/s1
InChI key
UPXRTVAIJMUAQR-BTYIYWSLSA-N
Related Categories
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
Certificates of Analysis (COA)
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Articles
Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.
Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.
Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.
Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.
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