All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C12H13NO2
CAS Number:
Molecular Weight:
203.24
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
assay
97%
bp
158-160 °C/0.2 mmHg (lit.)
mp
55-59 °C (lit.)
solubility
methylene chloride: soluble
SMILES string
O=C1CCN(CC1)C(=O)c2ccccc2
InChI
1S/C12H13NO2/c14-11-6-8-13(9-7-11)12(15)10-4-2-1-3-5-10/h1-5H,6-9H2
InChI key
NZAXGZYPZGEVBD-UHFFFAOYSA-N
Application
1-Benzoyl-4-piperidone can be used as starting reagent in the synthesis of fentanyl.
Biochem/physiol Actions
1-Benzoyl-4-piperidone and 1-methyl-4-piperidone reacts with triethyl phosphono-acetate in the presence of excess base and yields both the endocyclic and exocyclic olefins[1].
Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
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.
Endocyclic vs exocyclic olefin formation from 4-piperidones via the wittig reaction.
Borne RF and Aboul-Enein HY.
Journal of Heterocyclic Chemistry, 9(4), 869-873 (1972)
Active Filters
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
