CAS 97944-45-1
:2-Chloro-5-methyl-4-nitropyridine
Description:
2-Chloro-5-methyl-4-nitropyridine is a heterocyclic organic compound characterized by a pyridine ring substituted with a chlorine atom, a methyl group, and a nitro group. The presence of these substituents influences its chemical properties and reactivity. The chlorine atom, being electronegative, can enhance the compound's electrophilic character, while the nitro group is a strong electron-withdrawing group, which can affect the compound's acidity and reactivity in nucleophilic substitution reactions. This compound typically appears as a yellow to brown solid and is soluble in organic solvents. It is often used in the synthesis of pharmaceuticals and agrochemicals due to its ability to participate in various chemical reactions, including electrophilic aromatic substitution and nucleophilic attacks. Safety precautions should be taken when handling this compound, as it may pose health risks, including potential toxicity and environmental hazards. Proper storage and disposal methods are essential to mitigate any risks associated with its use.
Formula:C6H5ClN2O2
InChI:InChI=1S/C6H5ClN2O2/c1-4-3-8-6(7)2-5(4)9(10)11/h2-3H,1H3
InChI key:InChIKey=PEGDFBBVKXPIME-UHFFFAOYSA-N
SMILES:N(=O)(=O)C=1C(C)=CN=C(Cl)C1
Synonyms:- Pyridine,2-chloro-5-methyl-4-nitro
- Qc-6657
- 2-Chloro-5-methyl-4-nitropyridine
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Found 5 products.
Pyridine, 2-chloro-5-methyl-4-nitro-
CAS:Formula:C6H5ClN2O2Purity:95%Color and Shape:SolidMolecular weight:172.56912-Chloro-5-methyl-4-nitropyridine
CAS:<p>2-Chloro-5-methyl-4-nitropyridine</p>Purity:97%Molecular weight:172.57g/mol2-Chloro-5-methyl-4-nitropyridine
CAS:<p>2-Chloro-5-methyl-4-nitropyridine is a compound that has an intense yellow color. It has the chemical formula of C6H3ClN2O2. This molecule belongs to the group of heterocyclic compounds and contains a nitrogen atom with two substituents, one chloro, and one methyl group. The energy levels for this molecule are determined by its transition energies, which vary depending on the substitution patterns and electronic spectra. For example, if it has substituents at the 2 position, then its uv spectrum will have a maximum in the region of 230 nm. The electronic spectra for this molecule is characterized by transitions from the singlet state to the triplet state. In addition to these properties, 2-chloro-5-methyl-4-nitropyridine possesses n-oxides as well as an electron spin resonance (ESR) spectrum that contains peaks at g = 3/2 and g</p>Formula:C6H5ClN2O2Purity:Min. 95%Molecular weight:172.57 g/mol




