15115
Boc-Glu-OPh
≥98.0% (TLC)
Synonym(s):
Boc-L-glutamic acid 1-phenyl ester
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C16H21NO6
CAS Number:
Molecular Weight:
323.34
PubChem Substance ID:
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
7340685
MDL number:
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
assay
≥98.0% (TLC)
reaction suitability
reaction type: Boc solid-phase peptide synthesis
application(s)
peptide synthesis
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service