CAS 59146-96-2

2,3-dimethyl-6-nitroaniline

Description:

2,3-Dimethyl-6-nitroaniline is an organic compound characterized by its aromatic amine structure, which includes a nitro group and two methyl substituents on the benzene ring. The presence of the nitro group (–NO2) introduces significant polarity and reactivity, making this compound useful in various chemical applications, including dye synthesis and as an intermediate in organic synthesis. The methyl groups (–CH3) at the 2 and 3 positions contribute to the compound's hydrophobic characteristics and influence its electronic properties. Typically, this compound appears as a solid at room temperature and may exhibit moderate solubility in organic solvents. Its chemical behavior is influenced by the electron-withdrawing nature of the nitro group, which can affect nucleophilic substitution reactions. Safety considerations are important, as nitroanilines can be hazardous, and appropriate handling and disposal methods should be employed. Overall, 2,3-dimethyl-6-nitroaniline serves as a valuable compound in chemical research and industrial applications.

Formula: C₈H₁₀N₂O₂

InChI: InChI=1/C8H10N2O2/c1-5-3-4-7(10(11)12)8(9)6(5)2/h3-4H,9H2,1-2H3

SMILES: Cc1ccc(c(c1C)N)N(=O)=O

6-Nitro-2,3-xylidine

CAS: 59146-96-2

Formula: C₈H₁₀N₂O₂

Purity: >98.0%(GC)

Color and Shape: Orange to Brown to Dark red powder to crystal

Molecular weight: 166.18

Ref: 3B-N0500

2,3-Dimethyl-6-nitroaniline

CAS: 59146-96-2

Formula: C₈H₁₀N₂O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 166.1772

Ref: IN-DA003FK5

2,3-Dimethyl-6-nitroaniline

CAS: 59146-96-2

2,3-Dimethyl-6-nitroaniline

Formula: C₈H₁₀N₂O₂

Purity: ≥95%

Color and Shape: yellow-brown solid

Molecular weight: 166.18g/mol

Ref: 54-OR28632

2,3-Dimethyl-6-nitroaniline

CAS: 59146-96-2

Formula: C₈H₁₀N₂O₂

Purity: 97%

Color and Shape: Solid, Reddish yellow to deep reddish yellow powder

Molecular weight: 166.18

Ref: 10-F330097

6-Nitro-2,3-xylidine

CAS: 59146-96-2

6-Nitro-2,3-xylidine is a molecule that has been synthesized using organocatalytic methods. This compound is an electron acceptor and a strong nucleophile, which can be used for the synthesis of chiral derivatives. As an organocatalyst, 6-nitro-2,3-xylidine can be used to sulfonate aldehydes with high stereoselectivity. The molecular orbital diagram shows that the antibonding interaction is stronger than the bonding interaction between this compound and chloride.

Formula: C₈H₁₀N₂O₂

Purity: Min. 95%

Molecular weight: 166.18 g/mol

Ref: 3D-JCA14696