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Merck
CN

09774

Fmoc-Bpa-OH

≥98.0%

Synonym(s):

Fmoc-4-benzoyl-L-phenylalanine

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About This Item

Empirical Formula (Hill Notation):
C31H25NO5
CAS Number:
117666-96-3
Molecular Weight:
491.53
Beilstein:
7672022
MDL number:
MFCD00151937
UNSPSC Code:
12352209
PubChem Substance ID:
329748821
NACRES:
NA.26

Key Documents

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Quality Level

100

Assay

≥98.0%

form

powder

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

color

white

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

OC(=O)[C@H](Cc1ccc(cc1)C(=O)c2ccccc2)NC(=O)OCC3c4ccccc4-c5ccccc35

InChI

1S/C31H25NO5/c33-29(21-8-2-1-3-9-21)22-16-14-20(15-17-22)18-28(30(34)35)32-31(36)37-19-27-25-12-6-4-10-23(25)24-11-5-7-13-26(24)27/h1-17,27-28H,18-19H2,(H,32,36)(H,34,35)/t28-/m0/s1

InChI key

SYOBJKCXNRQOGA-NDEPHWFRSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF9251
BCCD2995
BCBV6872

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Xue Zhi Zhao et al.
Molecules (Basel, Switzerland), 23(8) (2018-07-28)
HIV-1 integrase (IN) inhibitors represent a new class of highly effective anti-AIDS therapeutics. Current FDA-approved IN strand transfer inhibitors (INSTIs) share a common mechanism of action that involves chelation of catalytic divalent metal ions. However, the emergence of IN mutants

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