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Merck
CN

532592

4-Methyl-3-nitropyridine

97%

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About This Item

Empirical Formula (Hill Notation):
C6H6N2O2
CAS Number:
Molecular Weight:
138.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
solid
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InChI key

JLNRJMGYBKMDGI-UHFFFAOYSA-N

SMILES string

Cc1ccncc1[N+]([O-])=O

InChI

1S/C6H6N2O2/c1-5-2-3-7-4-6(5)8(9)10/h2-4H,1H3

assay

97%

form

solid

refractive index

n20/D 1.549

bp

238 °C

mp

24-28 °C

density

1.228 g/mL at 25 °C

Application

4-Methyl-3-nitropyridine may be used as a starting material in the synthesis of ethyl 6-azaindole-2-carboxylate and also 3-substituted azaindoles.

General description

4-Methyl-3-nitropyridine, a substituted nitropyridine, can be prepared by the malonation of 4-methoxy-3-nitropyridine with sodium diethyl malonate.

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

226.9 °F - closed cup

flash_point_c

108.3 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Regulatory Information

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Pyridine derivatives: PART VI Malonations of substituted nitropyridines.
Gruber W.
Canadian Journal of Chemistry, 31(12), 1181-1188 (1953)
Synthesis and reactivity of 4-, 5-and 6-azaindoles.
Popowycz F, et al.
Tetrahedron, 63(36), 8689-8707 (2007)

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