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
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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.
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