2-Nitrocyclohexanone

Name: 2-Nitrocyclohexanone
Brand: ALDRICH
Price: 273 USD
Availability: InStock

99%

Synonym(s):

α-Nitrocyclohexanone, 2-Nitrocyclohexan-1-one, 2-Nitrocyclohexanone

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5 G

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About This Item

Linear Formula:

O₂NC₆H₉(=O)

CAS Number:

4883-67-4

Molecular Weight:

143.14

MDL number:

MFCD00001627

UNSPSC Code:

12352100

PubChem Substance ID:

24853441

NACRES:

NA.22

Key Documents

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assay

99%

form

solid

mp

39-43 °C (lit.)

functional group

ketone
nitro

SMILES string

[O-][N+](=O)C1CCCCC1=O

InChI

1S/C6H9NO3/c8-6-4-2-1-3-5(6)7(9)10/h5H,1-4H2

InChI key

SZNILIWUUKKNPE-UHFFFAOYSA-N

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1 of 4

This Item	299553	225088	292494
Sigma-Aldrich 224480 2-Nitrocyclohexanone	Sigma-Aldrich 299553 2-Acetyl-5-methylfuran	Sigma-Aldrich 225088 5-Amino-2-methylphenol	Sigma-Aldrich 292494 5-Chloro-2-methoxybenzoic acid
assay 99%	assay 98%	assay 97%	assay 99%
form solid	form liquid	form -	form -
mp 39-43 °C (lit.)	mp -	mp 160-162 °C (lit.)	mp 98-100 °C (lit.)
functional group ketone	functional group ketone	functional group -	functional group carboxylic acid, chloro

General description

The tautomerization rates of 2-nitrocyclohexanone (2-NCH) has been studied spectrophotometrically in several organic aprotic solvents and their binary mixtures[1].

pictograms

GHS07

signalword

Warning

hcodes

H302,H319

pcodes

P264 - P280 - P301 + P312 - P305 + P351 + P338 - P337 + P313 - P501

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Solvent effects on the rate of the keto-enol interconversion of 2-nitrocyclohexanone.

Gabriella Siani et al.

Organic & biomolecular chemistry, 6(22), 4236-4241 (2008-10-31)

The rates of tautomerization of 2-nitrocyclohexanone (2-NCH) have been measured spectrophotometrically at 25.0 +/- 0.1 degrees C in several organic aprotic solvents and their binary mixtures. In cyclohexane the reaction is effectively catalyzed by bases and inhibited by acids while

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2-Nitrocyclohexanone