V209
δ-Valerolactam
98%
Synonym(s):
delta-Valerolactam, 2-Piperidone
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About This Item
Empirical Formula (Hill Notation):
C5H9NO
CAS Number:
Molecular Weight:
99.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-622-9
Beilstein/REAXYS Number:
106434
MDL number:
Product Name
δ-Valerolactam, 98%
InChI key
XUWHAWMETYGRKB-UHFFFAOYSA-N
InChI
1S/C5H9NO/c7-5-3-1-2-4-6-5/h1-4H2,(H,6,7)
SMILES string
O=C1CCCCN1
assay
98%
bp
256 °C (lit.)
81-82 °C/0.1 mmHg (lit.)
mp
38-40 °C (lit.)
Quality Level
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Related Categories
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
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S Gordon et al.
Farmaco (Societa chimica italiana : 1989), 52(10), 603-608 (1998-05-15)
The synthesis of a series of 2-amino-4-hydroxy-delta-valerolactam derivatives is described (compounds 4 to 10). These compounds showed a high anthelmintic in vitro activity against the Nippostrongylus brasiliensis model.
Zheng Hu et al.
Chemosphere, 268, 128834-128834 (2020-11-11)
A magnetic Ag3PO4/rGO/CoFe2O4 ternary catalyst was firstly prepared and used for removing levofloxacin (LVF) from different water matrices via simultaneous adsorption and photocatalysis. Compared with Ag3PO4 and Ag3PO4/CoFe2O4, Ag3PO4/rGO/CoFe2O4 shows a superior adsorption-photocatalysis performance for LVF elimination since rGO component
Hiroshi Tsuchikawa et al.
Organic letters, 14(9), 2326-2329 (2012-04-26)
Chiral 2-piperidinone compounds with various C-6 substituents were successfully synthesized via a Pd-catalyzed asymmetric 6-endo cyclization of dienamides, which were evidently activated by both N-p-toluenesulfonyl and C-3 ester substituents.
Asymmetric synthesis of gamma-keto-delta-lactam derivatives: application to the synthesis of a conformationally constrained surrogate of Ala-Ser dipeptide.
S D Koulocheri et al.
The Journal of organic chemistry, 66(23), 7915-7918 (2001-11-10)
Metabolic engineering of Escherichia coli for the production of four-, five- and six-carbon lactams.
Tong Un Chae et al.
Metabolic engineering, 41, 82-91 (2017-04-10)
Microbial production of chemicals and materials from renewable sources is becoming increasingly important for sustainable chemical industry. Here, we report construction of a new and efficient platform metabolic pathway for the production of four-carbon (butyrolactam), five-carbon (valerolactam) and six-carbon (caprolactam)
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