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2-Nitro-cyclohexanone oxime is an organic compound with the molecular formula C6H10N2O3. It is derived from cyclohexanone, a cyclic ketone, by introducing a nitro group at the 2-position and an oxime group. 2-nitro-cyclohexanone oxime is characterized by its yellow crystalline appearance and is soluble in organic solvents. It is synthesized through a series of chemical reactions, including the nitration of cyclohexanone followed by the formation of the oxime. 2-Nitro-cyclohexanone oxime is used as an intermediate in the synthesis of various pharmaceuticals and chemical compounds, particularly in the production of certain drugs and agrochemicals. Its reactivity and functional groups make it a valuable building block in organic chemistry.

2209-34-9

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2209-34-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2209-34-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2209-34:
(6*2)+(5*2)+(4*0)+(3*9)+(2*3)+(1*4)=59
59 % 10 = 9
So 2209-34-9 is a valid CAS Registry Number.

2209-34-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-nitro-cyclohexanone oxime

1.2 Other means of identification

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Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

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More Details:2209-34-9 SDS

2209-34-9Upstream product

2209-34-9Relevant academic research and scientific papers

Amberlyst A-21 an excellent heterogeneous catalyst for the conversion of carbonyl compounds to oximes

Ballini, Roberto,Barboni, Luciano,Filippone, Paolino

, p. 475 - 476 (2007/10/03)

Oximes can be efficiently obtained at room temperature by simply dissolving the appropriate carbonyl compounds and hydroxylamine hydrochloride, in ethanol, with Amberlyst A-21 as catalyst. Good yields of oximes are obtained, in very short reaction times, even with polifunctionalized substrates.

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