Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C13H21NO5
CAS Number:
Molecular Weight:
271.31
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
Product Name
Ethyl (R)-1-Boc-4-oxopiperidine-2-carboxylate, 97%
InChI
1S/C13H21NO5/c1-5-18-11(16)10-8-9(15)6-7-14(10)12(17)19-13(2,3)4/h10H,5-8H2,1-4H3/t10-/m1/s1
SMILES string
CCOC(=O)[C@H]1CC(=O)CCN1C(=O)OC(C)(C)C
InChI key
YAVQLRUBKDCOCI-SNVBAGLBSA-N
assay
97%
form
solid
mp
42-47 °C
functional group
ester
ketone
storage temp.
2-8°C
Quality Level
Related Categories
Application
Ethyl (R)-1-Boc-4-oxopiperidine-2-carboxylate can be used as a key intermediate in the preparation of 4-oxopipecolic acid enantiomer, a non-proteinogenic amino acid having antibiotic activity.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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.
Practical synthesis of both enantiomers of protected 4-oxopipecolic acid
Machetti F, et al.
Tetrahedron, 57(23), 4995-4998 (2001)
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