20430
Boc-OSu
≥98.0% (CHN), for peptide synthesis
Synonym(s):
N-(tert-Butoxycarbonyloxy)succinimide, tert-Butyl N-succinimidyl carbonate
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About This Item
Empirical Formula (Hill Notation):
C9H13NO5
CAS Number:
Molecular Weight:
215.20
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352005
EC Number:
236-071-1
MDL number:
Beilstein/REAXYS Number:
1536756
Product Name
Boc-OSu, ≥98.0% (CHN)
InChI key
VTGFSVGZCYYHLO-UHFFFAOYSA-N
InChI
1S/C9H13NO5/c1-9(2,3)14-8(13)15-10-6(11)4-5-7(10)12/h4-5H2,1-3H3
SMILES string
CC(C)(C)OC(=O)ON1C(=O)CCC1=O
assay
≥98.0% (CHN)
form
solid
mp
~95 °C (dec.)
application(s)
peptide synthesis
functional group
imide
storage temp.
−20°C
Quality Level
Other Notes
Boc-protecting group reagent
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Skin Sens. 1
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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M. Franke et al.
Tetrahedron Letters, 4765-4765 (1966)
Stabilization of Bacillus subtilis -amylase by amino group acylation.
J Hora
Biochimica et biophysica acta, 310(1), 264-267 (1973-05-17)
H. Gross et al.
Justus Liebigs Annalen der Chemie, 725, 212-212 (1969)
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