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Merck
CN

C102202

Cyclohexanone oxime

97%

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About This Item

Linear Formula:
C6H10(=NOH)
CAS Number:
Molecular Weight:
113.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-874-0
Beilstein/REAXYS Number:
1616769
MDL number:
Assay:
97%
Form:
crystals
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Product Name

Cyclohexanone oxime, 97%

InChI key

VEZUQRBDRNJBJY-UHFFFAOYSA-N

InChI

1S/C6H11NO/c8-7-6-4-2-1-3-5-6/h8H,1-5H2

SMILES string

O\N=C1/CCCCC1

assay

97%

form

crystals

bp

206-210 °C (lit.)

mp

86-89 °C (lit.)

Quality Level

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pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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S C Gad et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 5(1), 128-136 (1985-02-01)
Dermal exposure of rabbits to cyclohexanone oxime (CHO) for 24 hr at 0, 0.8, 2, and 5 g/kg caused dose-related reticulocytosis on the day after dosing as well as a decrease in hemoglobin in the 5-g/kg females 7 days postdosing.
Shelli J Schomaker et al.
Toxicology and applied pharmacology, 185(1), 48-54 (2002-12-04)
The purpose of these studies was to evaluate bone marrow from male CD rats following exposure to known hematotoxins using flow cytometry (FC) and a monoclonal antibody to the cell surface antigen CD71. Rats were treated with either CHO (300
Wen-Cui Li et al.
Journal of the American Chemical Society, 127(36), 12595-12600 (2005-09-08)
In this study, we present a synthetic pathway for the fabrication of self-supporting zeolite monoliths consisting of crystallized nanoparticles. A resorcinol-formaldehyde-based organic aerogel is used as a template, and silicalite-1 is used as the zeolite example. The silicalite-1 monoliths obtained
Raphaël Turgis et al.
ChemSusChem, 3(12), 1403-1408 (2010-12-01)
Brønsted-acidic ionic liquids that bear a sulfonic acid group, known as Forbes acids, show a good catalytic activity for the Beckmann rearrangement, used to prepare ε-caprolactam, which is a precursor of Nylon 6. The activity essentially stems from the acidity of
S Ramalingam et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 96, 207-220 (2012-06-12)
In the present analysis, FT-IR/FT-Raman spectra of the cyclohexanone oxime (CHO, C(6)H(11)NO) are recorded. The observed vibrational frequencies are assigned and the computational calculations are carried out by HF and DFT (B3LYP and B3PW91) methods with 6-311++G(d,p) basis set and

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