193216
2-Chloronicotinamide
98%
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About This Item
Empirical Formula (Hill Notation):
C6H5ClN2O
CAS Number:
Molecular Weight:
156.57
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
233-808-9
MDL number:
Assay:
98%
Form:
solid
InChI key
ZQZAHPFFZWEUCL-UHFFFAOYSA-N
InChI
1S/C6H5ClN2O/c7-5-4(6(8)10)2-1-3-9-5/h1-3H,(H2,8,10)
SMILES string
NC(=O)c1cccnc1Cl
assay
98%
form
solid
mp
164-167 °C (lit.)
Application
2-Chloronicotinamide was used in the synthesis of pyrrolopyridines and thiol ester derived from 2-mecaptonicotinamide.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Benzyl and tert Butyl Sulfoxides as Sulfenyl Halide Equivalents: a Convenient Preparation of Benzisothiazolones.
Wright SW, et al.
Tetrahedron Letters, 33, 153-156 (1992)
Microwave assisted copper-free Sonogashira coupling/5-exo-dig cycloisomerization domino reaction: access to 3-(phenylmethylene) isoindolin-1-ones and related heterocycles.
Hellal M and Cuny GD.
Tetrahedron Letters, 52(42), 5508-5511 (2011)
D R Schneider et al.
Infection and immunity, 38(2), 548-553 (1982-11-01)
Several conditions of growth of Bordetella pertussis cause a reversible phenotypic alteration in properties termed modulation. Growth in medium containing nicotinic acid induces normal (X-mode) cells to change to modulated (C-mode) cells. We examined several pyridines and compounds resembling pyridines
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