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Merck
CN

15469

Boc-Homophe-OH

≥98.0% (TLC)

Synonym(s):

(S)-2-(Boc-amino)-4-phenylbutyric acid, Boc-L-homophenylalanine

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About This Item

Linear Formula:
C6H5CH2CH2CH[NHCOOC(CH3)3]COOH
CAS Number:
100564-78-1
Molecular Weight:
279.33
UNSPSC Code:
12352202
NACRES:
NA.22
PubChem Substance ID:
57647444
MDL number:
MFCD00076904
Beilstein/REAXYS Number:
3653506

Key Documents

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Product Name

Boc-Homophe-OH, ≥98.0% (TLC)

InChI

1S/C15H21NO4/c1-15(2,3)20-14(19)16-12(13(17)18)10-9-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,16,19)(H,17,18)/t12-/m0/s1

SMILES string

CC(C)(C)OC(=O)N[C@@H](CCc1ccccc1)C(O)=O

InChI key

MCODLPJUFHPVQP-LBPRGKRZSA-N

assay

≥98.0% (TLC)

form

powder

optical activity

[α]20/D +6.5±1°, c = 2% in ethanol

reaction suitability

reaction type: Boc solid-phase peptide synthesis

mp

76-80 °C

application(s)

peptide synthesis

storage temp.

2-8°C

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ9475
BCCF7842
BCBZ3796
BCBX6423
BCBQ2667V

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R Voegeli et al.
International journal of cosmetic science, 39(2), 109-120 (2016-07-20)
The aim of this study was to optimize the synthesis of the plasmin and urokinase (uPA) inhibitor benzylsulfonyl-D-Ser-homoPhe-(4-amidino-benzylamide) (BSFAB), to characterize its activity and mechanism of action and to assess its use to improve stratum corneum (SC) barrier function. Peptide

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