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Merck
CN

15490

Boc-Pro-OH

≥99.0% (T)

Synonym(s):

N-(tert-Butoxycarbonyl)-L-proline, Boc-L-proline

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About This Item

Empirical Formula (Hill Notation):
C10H17NO4
CAS Number:
15761-39-4
Molecular Weight:
215.25
NACRES:
NA.22
PubChem Substance ID:
57647368
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
239-848-3
MDL number:
MFCD00037324
Beilstein/REAXYS Number:
15828

Key Documents

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Product Name

Boc-Pro-OH, ≥99.0% (T)

InChI key

ZQEBQGAAWMOMAI-ZETCQYMHSA-N

InChI

1S/C10H17NO4/c1-10(2,3)15-9(14)11-6-4-5-7(11)8(12)13/h7H,4-6H2,1-3H3,(H,12,13)/t7-/m0/s1

SMILES string

CC(C)(C)OC(=O)N1CCC[C@H]1C(O)=O

assay

≥99.0% (T)

form

solid

optical activity

[α]20/D −61±2°, c = 2% in acetic acid

reaction suitability

reaction type: Boc solid-phase peptide synthesis

mp

133-135 °C (lit.)

application(s)

peptide synthesis

Quality Level

100

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Related Categories

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF6620V
WXBF3798V
BCCH0480
BCCC9557
BCBZ3528

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Manos Gkikas et al.
Biomacromolecules, 16(11), 3686-3693 (2015-10-16)
Novel poly(L-lysine)-block-poly(L-proline) (PLL-b-PLP)-based materials with all PLP helical conformers, i.e., PLP II and the rare PLP I are here reported. Electrostatic supramolecular complexation of the adjacent cationic PLL with anionic molecules bearing DNA analogue H-bonding functionalities, such as deoxyguanosine monophosphate
Griet Van Zeebroeck et al.
Nature chemical biology, 5(1), 45-52 (2008-12-09)
Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting transceptors is unknown. We have screened 319 amino acid analogs to identify compounds that act on Gap1

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Proline Derivatives and Analogs

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