CAS 3230-35-1

2-Naphthalenamine,6-nitro-

Description:

2-Naphthalenamine, 6-nitro- is an organic compound characterized by its structure, which consists of a naphthalene ring substituted with an amino group and a nitro group. The presence of the amino group (-NH2) makes it an amine, while the nitro group (-NO2) is a strong electron-withdrawing group that can influence the compound's reactivity and properties. This compound is typically a solid at room temperature and may exhibit a yellow to brown color due to the nitro substitution. It is soluble in organic solvents but has limited solubility in water. 2-Naphthalenamine, 6-nitro- can participate in various chemical reactions, including electrophilic aromatic substitution and reduction reactions, making it useful in organic synthesis and potentially in the production of dyes or pharmaceuticals. However, like many nitro compounds, it may pose environmental and health risks, necessitating careful handling and disposal. Always refer to safety data sheets and regulatory guidelines when working with such substances.

Formula: C₁₀H₈N₂O₂

InChI: InChI=1S/C10H8N2O2/c11-9-3-1-8-6-10(12(13)14)4-2-7(8)5-9/h1-6H,11H2

InChI key: LNYJXDMWSMEVGQ-UHFFFAOYSA-N

SMILES: C1=CC2=C(C=CC(=C2)[N+](=O)[O-])C=C1N

Synonyms:

• 2-Naphthylamine,6-nitro- (7CI,8CI)
• 2-Amino-6-nitronaphthalene

6-Nitronaphthalen-2-amine

CAS: 3230-35-1

Formula: C₁₀H₈N₂O₂

Purity: 96%

Color and Shape: Solid

Molecular weight: 188.1827

Ref: IN-DA00CLMO

6-Nitronaphthalen-2-amine

CAS: 3230-35-1

6-Nitronaphthalen-2-amine

Formula: C₁₀H₈N₂O₂

Purity: 96%

Molecular weight: 188.19

Ref: 54-OR1066557

6-Nitronaphthalen-2-amine

CAS: 3230-35-1

6-Nitronaphthalen-2-amine is a triazolium salt that is used as an intermediate in the synthesis of dyestuffs and other nitrogenous compounds. It is prepared by the reaction of sodium hypochlorite with aminobenzene in the presence of aniline and hydroxylamine. The compound has a characteristic spectrum consisting of a doublet at δ 8.0, due to the two nitro groups, and a triplet at δ 7.0, due to the three aminotriazole groups. The compound also reacts with sodium hypochlorite to produce 6-nitronaphthalen-1-amine (6NNA), which can be used as an oxidizing agent. The reaction scheme is shown below:

Formula: C₁₀H₈N₂O₂

Purity: Min. 95 Area-%

Color and Shape: Powder

Molecular weight: 188.18 g/mol

Ref: 3D-DAA23035

6-Nitronaphthalen-2-amine

CAS: 3230-35-1

6-Nitronaphthalen-2-amine

Formula: C₁₀H₈N₂O₂

Purity: 96%

Molecular weight: 188.18

Ref: IN-DG256373