30950-32-4 Usage
General Description
"(E)-1-(cyclohex-1-en-1-yl)-N-hydroxymethanimine" is a chemical compound with the molecular formula C7H11NO. It is a hydroxylamine derivative with a cyclohexene group attached to a hydroxymethanimine functional group. (E)-1-(cyclohex-1-en-1-yl)-N-hydroxymethanimine can be used as a reagent in organic synthesis and is also of interest in pharmaceutical and medicinal chemistry due to its potential biological activity. It is important to handle and store this compound with care, as it may be hazardous if not used properly. Further research and experimentation are needed to fully understand the properties and potential applications of this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 30950-32-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,9,5 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 30950-32:
(7*3)+(6*0)+(5*9)+(4*5)+(3*0)+(2*3)+(1*2)=94
94 % 10 = 4
So 30950-32-4 is a valid CAS Registry Number.
30950-32-4Relevant articles and documents
Grignard reaction of substituted nitromethanes: The nwe observations
Gupta, Ramesh Chandra,Seth, M,Bhaduri, A P
, p. 745 - 747 (2007/10/02)
Reactions of 1-(1-nitromethyl)cyclohexene and its derivatives with excess of methylmagnesium iodide have been studied.In a few cases a chemoselective attack on the nitro group by the Grignard reagent has been observed.The N,N-dialkylhydroxylamine, the nor
One-pot Conversion of Allylic Nitro Compounds Into Nitriles with Carbon Disulphide under Phase-transfer Catalysis Conditions
Albanese, Domenico,Landini, Dario,Penso, Michele,Pozzi, Gianluca
, p. 965 - 971 (2007/10/02)
An one-pot synthesis of allylic nitriles 3 from the corresponding nitro derivatives 1 is described.In the first step the substrates 1 are reduced to the oximes 2 by carbon disulphide in the presence of wet potassium carbonate, in solid-liquid PTC conditions.In the second, the formed oximes 2 are dehydrated by adding more CS2 and 15percent aqueous NaOH.
