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Merck
CN

421707

Boc-Phe-OMe

98%

Synonym(s):

N-(tert-Butoxycarbonyl)-L-phenylalanine methyl ester, Boc-L-phenylalanine methyl ester

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About This Item

Linear Formula:
C6H5CH2CH[NHCO2C(CH3)3]CO2CH3
CAS Number:
51987-73-6
Molecular Weight:
279.33
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
24866397
MDL number:
MFCD00076977
Beilstein/REAXYS Number:
3061910

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InChI

1S/C15H21NO4/c1-15(2,3)20-14(18)16-12(13(17)19-4)10-11-8-6-5-7-9-11/h5-9,12H,10H2,1-4H3,(H,16,18)/t12-/m0/s1

SMILES string

COC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C

InChI key

SDSWSVBXRBXPRL-LBPRGKRZSA-N

assay

98%

optical activity

[α]22/D −4.0°, c = 2 in methanol

reaction suitability

reaction type: Boc solid-phase peptide synthesis

mp

36-40 °C (lit.)

application(s)

peptide synthesis

Quality Level

200

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pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number
0000259975
0000246010
0000259975
0000246010
MKBD0399

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Natashya Falcone et al.
Chembiochem : a European journal of chemical biology, 20(6), 838-845 (2018-12-01)
Nicotinamide and pyridine-containing conjugates have attracted a lot of attention in research as they have found use in a wide range of applications including as redox flow batteries and calcium channel blockers, in biocatalysis, and in metabolism. The interesting redox

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