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Merck
CN

15115

Sigma-Aldrich

Boc-Glu-OPh

≥98.0% (TLC)

Synonym(s):

Boc-L-glutamic acid 1-phenyl ester

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About This Item

Empirical Formula (Hill Notation):
C16H21NO6
CAS Number:
Molecular Weight:
323.34
Beilstein:
7340685
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
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Assay

≥98.0% (TLC)

reaction suitability

reaction type: Boc solid-phase peptide synthesis

application(s)

peptide synthesis

SMILES string

CC(C)(C)OC(=O)N[C@@H](CCC(O)=O)C(=O)Oc1ccccc1

InChI

1S/C16H21NO6/c1-16(2,3)23-15(21)17-12(9-10-13(18)19)14(20)22-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,17,21)(H,18,19)/t12-/m0/s1

InChI key

UUGORLVQLJSWBX-LBPRGKRZSA-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

Regulatory Information

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C J Bailey et al.
The Biochemical journal, 284 ( Pt 1), 177-180 (1992-05-15)
The two epidermolytic toxins were shown to have intrinsic N-t-butyloxycarbonyl-L-glutamic acid alpha-phenyl esterase activity. The activity was dependent on free toxin pKa values of 6.6 and 6.8 for ETA and ETB respectively. ETB incorporated 0.97 mol of radiolabelled di-isopropyl phosphorofluoridate/mol

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