Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

17346

Sigma-Aldrich

Ethyl N-Boc-oxamidate

≥97.0%

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Empirical Formula (Hill Notation):
C9H15NO5
CAS Number:
216959-34-1
Molecular Weight:
217.22
Beilstein:
8201747
MDL number:
MFCD01631201
UNSPSC Code:
12352108
PubChem Substance ID:
57647637
NACRES:
NA.22

Assay

≥97.0%

form

solid

refractive index

n20/D 1.449

application(s)

peptide synthesis

functional group

amide
ester

storage temp.

−20°C

SMILES string

CCOC(=O)C(=O)NC(=O)OC(C)(C)C

InChI

1S/C9H15NO5/c1-5-14-7(12)6(11)10-8(13)15-9(2,3)4/h5H2,1-4H3,(H,10,11,13)

InChI key

DSDQWJVXMDHQLK-UHFFFAOYSA-N

Other Notes

Reagent for transforming alcohols into BOC-protected amines by Mitsunobu reaction (PPh3/DEAD); prim and sec alcohols (inversion of configuration) give good yields

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Hazard Classifications

Acute Tox. 4 Oral

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
1057478
63642/1
063642/1

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

F. Berree et al.
Tetrahedron Letters, 39, 8275-8275 (1998)

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