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213381

Sigma-Aldrich

Nicotinoyl chloride hydrochloride

97%

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About This Item

Fórmula empírica (notación de Hill):
C6H4ClNO · HCl
Número de CAS:
20260-53-1
Peso molecular:
178.02
EC Number:
243-648-1
MDL number:
MFCD00012820
UNSPSC Code:
12352100
PubChem Substance ID:
24852779
NACRES:
NA.22

assay

97%

form

powder

mp

151-157 °C (lit.)

functional group

acyl chloride

SMILES string

Cl[H].ClC(=O)c1cccnc1

InChI

1S/C6H4ClNO.ClH/c7-6(9)5-2-1-3-8-4-5;/h1-4H;1H

InChI key

MSYBLBLAMDYKKZ-UHFFFAOYSA-N

Categorías relacionadas

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

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

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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Certificados de análisis (COA)

Lot/Batch Number
0000378601
0000378601
MKCS4463
0000295280
0000184541

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Synthesis of bis(ethylenedithio) tetrathiafulvalene derivatives with metal ion ligating centres.
Griffiths J-P, et al.
Tetrahedron Letters, 44(15), 31327-31331 (2003)
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 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
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
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