CAS 3272-91-1

5-Nitro-1-naphthalenamine

Description:

5-Nitro-1-naphthalenamine, with the CAS number 3272-91-1, is an organic compound characterized by the presence of a nitro group (-NO2) and an amine group (-NH2) attached to a naphthalene ring system. This compound typically appears as a solid and is known for its yellow to orange coloration. It is soluble in organic solvents but has limited solubility in water. The nitro group contributes to its reactivity, making it a potential candidate for various chemical reactions, including electrophilic substitutions and reductions. 5-Nitro-1-naphthalenamine is often used in the synthesis of dyes, pigments, and pharmaceuticals due to its ability to undergo further chemical transformations. Additionally, it is important to handle this compound with care, as nitro compounds can be hazardous and may pose environmental risks. Proper safety measures should be observed when working with this substance in laboratory or industrial settings.

Formula: C₁₀H₈N₂O₂

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

InChI key: InChIKey=WEWILNPCZSSAIJ-UHFFFAOYSA-N

SMILES: N(=O)(=O)C=1C2=C(C(N)=CC=C2)C=CC1

Synonyms:

• 1-Amino-5-nitronaphthalene
• 1-Naphthalenamine, 5-Nitro-
• 1-Naphthylamine, 5-nitro-
• 1-Nitro-5-aminonaphthalene
• 5-Amino-1-nitro-naphthaline
• 5-Nitro-1-Naphthalenamine
• 5-Nitro-1-naphthylamine
• 5-Nitro-α-naphthylamine
• NSC 5522
• 5-Nitronaphthalen-1-amine
• 5-Nitro-alpha-naphthylamine
• 5-Nitro-naphthalen-1-ylamine

5-Nitronaphthalen-1-amine

CAS: 3272-91-1

Formula: C₁₀H₈N₂O₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 188.1827

Ref: IN-DA00CZFE

5-Nitronaphthalen-1-amine

CAS: 3272-91-1

5-Nitronaphthalen-1-amine

Purity: 95%

Molecular weight: 188.18g/mol

Ref: 54-OR914366

(5-Nitro-1-naphthyl)amine

CAS: 3272-91-1

Formula: C₁₀H₈N₂O₂

Color and Shape: Neat

Ref: TR-N233690

(5-Nitro-1-naphthyl)amine

CAS: 3272-91-1

(5-Nitro-1-naphthyl)amine is an aromatic amine that has been used as a dye and as a reagent in organic synthesis. (5-Nitro-1-naphthyl)amine has an electron withdrawing effect on the aromatic ring, which creates an electron rich environment. This allows it to undergo reductive elimination reactions with hydrochloric acid or hydrazine. It can also be converted into nitro groups by reduction with hydrogen and hydrochloric acid, or by oxidation with potassium permanganate. The intramolecular hydrogen bond of (5-nitro-1-naphthyl)amine is stronger than the intermolecular hydrogen bonding of the molecule with water molecules. This means that the solubility of (5-nitro-1-naphthyl)amine in water is low because it cannot easily form hydrogen bonds with other water molecules. The chromatographic separation of (5-nit

Formula: C₁₀H₈N₂O₂

Purity: Min. 95%

Color and Shape: Red Powder

Molecular weight: 188.18 g/mol

Ref: 3D-FN131372

(5-nitro-1-naphthyl)amine

CAS: 3272-91-1

Formula: C₁₀H₈N₂O₂

Purity: ≥95%

Molecular weight: 188.186

Ref: 10-F373612