213381
Nicotinoyl chloride hydrochloride
97%
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About This Item
Empirical Formula (Hill Notation):
C6H4ClNO · HCl
CAS Number:
Molecular Weight:
178.02
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
243-648-1
MDL number:
Product Name
Nicotinoyl chloride hydrochloride, 97%
InChI key
MSYBLBLAMDYKKZ-UHFFFAOYSA-N
InChI
1S/C6H4ClNO.ClH/c7-6(9)5-2-1-3-8-4-5;/h1-4H;1H
SMILES string
Cl[H].ClC(=O)c1cccnc1
assay
97%
form
powder
mp
151-157 °C (lit.)
functional group
acyl chloride
Quality Level
Related Categories
Application
Nicotinoyl chloride hydrochloride was used in the preparation of :
- 1-[5-O-tert-butyldimethylsilyl-2-deoxy-2-fluoro-3-O-(3-pyridylcarbonyl)-β-D-ribofuranosyl]uracil
- 7,16-dinicotinoylated and/or 7,16-diisonicotinoylated compounds via reaction with tetraaza[14]annulene and its complexes
- bis(ethylenedithio)tetrathiafulvalene derivatives
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Shuang Li et al.
Journal of the mechanical behavior of biomedical materials, 102, 103521-103521 (2019-12-27)
In this research, a bio-based monomer 1,3-bis(methacryloyloxy)propyl-carbonyl- hexylpyridinium bromide (QANMA) that derived from niacin was synthesized and incorporated into Bisphenol A glycidyl methacrylate (Bis-GMA)/triethylene glycol dimethacrylate (TEGDMA) (50 wt/50 wt) with a series of mass fraction as antibacterial agent. The double bond
Synthesis of bis(ethylenedithio) tetrathiafulvalene derivatives with metal ion ligating centres.
Griffiths J-P, et al.
Tetrahedron Letters, 44(15), 31327-31331 (2003)
K W Morin et al.
Carbohydrate research, 249(1), 109-116 (1993-10-18)
1-(2-Deoxy-2-fluoro-beta-D-ribofuranosyl-(E)-5-(2-iodovinyl)uracil (IVFRU) was coupled to a dihydropyridine <---> pyridinium salt redox chemical-delivery system (CDS) via a cleavable sugar-ester linkage as a site-directed approach to increase diffusion of the parent nucleoside into the central nervous system. Treatment of 1-(2-deoxy-2-fluoro-beta-D-ribofuranosyl)uracil with Bu(t)Me(2)SiCl
Synthesis and characterization of 7, 16-dinicotinoyl-and 7, 16-diisonico-tinoyltetraaza [14] annulene and their nickel (II) and copper (II) complexes.
Sakata K and Itoh M.
Journal of Heterocyclic Chemistry, 29(4), 921-926 (1992)
Wenqiang Tan et al.
Carbohydrate polymers, 157, 236-243 (2016-12-19)
Based on cuprous-catalyzed azide-alkyne cycloaddition (CuAAC), starch derivative bearing 1,2,3-triazole and pyridine (II) was prepared and subsequently followed by alkylation with iodomethane to synthesize starch derivative bearing 1,2,3-triazolium and pyridinium (III). The antifungal activities of starch derivatives against Colletotrichum lagenarium
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