30168-50-4 Usage
Explanation
1-methyl-1-nitrocyclopentane is composed of 6 carbon (C), 11 hydrogen (H), 1 nitrogen (N), and 2 oxygen (O) atoms.
Explanation
A nitro group is a functional group consisting of an oxygen-nitrogen-oxygen bond (-O-N=O) attached to a carbon atom, which is characteristic of nitro compounds.
Explanation
The cyclopentane ring is a five-carbon atom chain that forms a cyclic structure, which is a key component of 1-methyl-1-nitrocyclopentane.
Explanation
A methyl group (-CH3) is a carbon atom bonded to three hydrogen atoms, and in this compound, it is attached to the carbon atom next to the nitro group.
Explanation
1-methyl-1-nitrocyclopentane serves as a starting material or intermediate in the synthesis of various other organic compounds, making it a versatile chemical in chemical reactions.
Explanation
The compound has been studied for its ability to improve the performance of gasoline by increasing its octane rating, which is a measure of the fuel's resistance to knocking or premature ignition.
Explanation
1-methyl-1-nitrocyclopentane may have potential uses in the pharmaceutical industry for its potential medicinal properties, as well as in the agricultural industry for its pesticidal properties, although further research is needed to confirm these applications.
Nitro compound
Contains a nitro group (NO2)
Cyclopentane ring
Part of the molecular structure
Methyl group attachment
Adjacent to the nitro group
Precursor in organic synthesis
Used to produce other chemical compounds
Potential fuel additive
Increases octane rating of gasoline
Applications in pharmaceutical and agricultural industries
Medicinal and pesticidal properties
Check Digit Verification of cas no
The CAS Registry Mumber 30168-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,1,6 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 30168-50:
(7*3)+(6*0)+(5*1)+(4*6)+(3*8)+(2*5)+(1*0)=84
84 % 10 = 4
So 30168-50-4 is a valid CAS Registry Number.
30168-50-4Relevant articles and documents
Reduction of Substituted Nitro Compounds with Tri-n-butyltin Hydride
Bowman, W. Russell,Crosby, David,Westlake, Paul J.
, p. 73 - 80 (2007/10/02)
α-Substituted nitro compounds have been reduced with tri-n-butyltin hydride to give replacement of the α-substituent by hydrogen (2-bromo, 2-chloro- and 2-nitro-2-phenylsulphonylpropane to 2-nitropropane; p-nitrobenzyl chloride, bromide, iodide and thiocyanate to p-nitrotoluene; 5-nitrofurfuryl nitrate to 2-methyl-5-nitrofuran and 2-hydroxymethyl-5-nitrofuran; 2-(bromomethyl)-1-methyl-5-nitroimidazole to 1,2-dimethylimidazole). 2-Bromo-2-nitrohept-6-ene and 1-bromo-1-nitrohex-5-ene were reduced to 2-nitrohept-6-ene and 1-nitrohex-5-ene,5-bromo- and 5-phenylsulphonyl-5-nitro-6-phenyl-norborn-6-ene to 5-nitro-6-phenylnorborn-6-ene and 2-iodo-2-nitro-3-(endo-norborn-2-en-5-yl)propane to 2-nitro-3-(endo-norborn-2-en-5-yl)propane without cyclisation of the intermediate alkenyl α-nitroalkyl radicals. 2-Bromo-2-nitrohex-5-ene and 1-bromo-1-nitropent-4-ene were reduced to the respective nitroalkenes at high but at lower cyclisation to 1-methyl-1-nitrocyclopentane and 1-nitrocyclopentane took place.Inhibition studies of the reductions of 2-bromo-2-nitrohex-5-ene and p-nitrobenzyl bromide showed a radical chain mechanism.In some of the reductions at low , radical rearrangement of the intermediate α-nitroalkyl radicals gave the respective ketones.Mechanisms involving (a) addition/elimination and (b) dissociation of intermediate radical anions, are proposed.
