CAS 118-31-0

1-Naphthalenemethanamine

Description:

1-Naphthalenemethanamine, also known as 1-amino-2-naphthylmethane, is an organic compound characterized by its naphthalene structure with an amino group attached to a methylene bridge. It appears as a solid at room temperature and is typically colorless to pale yellow. This compound is known for its aromatic properties, which contribute to its stability and reactivity. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic naphthalene ring. 1-Naphthalenemethanamine is often used in the synthesis of dyes, pharmaceuticals, and other organic compounds, owing to its ability to participate in various chemical reactions, including electrophilic aromatic substitution. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, 1-Naphthalenemethanamine is a versatile compound with applications in both industrial and research settings.

Formula: C₁₁H₁₁N

InChI: InChI=1S/C11H11N/c12-8-10-6-3-5-9-4-1-2-7-11(9)10/h1-7H,8,12H2

InChI key: InChIKey=NVSYANRBXPURRQ-UHFFFAOYSA-N

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

Synonyms:

• (Naphthalen-1-ylmethyl)amine
• 1-(1-Naphthyl)methanamine
• 1-(1-Naphthyl)methylamine
• 1-(Aminomethyl)naphthalene
• 1-(Aminomethyl)naphthalene~1-Naphthylmethylamine
• 1-(Naphthalen-1-Yl)Methanamine
• 1-Naphthalenemethanamine
• 1-Naphthylmethanamine
• 1-Naphthylmethaneamine
• 1-Naphthylmethylamine
• C-(Naphthalen-1-yl)-methylamine
• NSC 210425
• Naphthalen-1-Ylmethanaminium
• Naphthalen-1-ylmethanamine
• α-Naphthylmethylamine

1-Naphthalenemethylamine, 98+%

CAS: 118-31-0

1-Naphthalenemethylamine is used to increase the induced circular dichroism (ICD) magnitude exhibited by poly[(4-carboxyphenyl)acetylene]. Further, it reacts with monomethoxypoly(ethylene glycol) succinimido carbonate to prepare carbamate. This Thermo Scientific Chemicals brand product was originall

Formula: C₁₁H₁₂N

Purity: 98+%

Color and Shape: Clear or slightly hazy, colorless to yellow to orange to red to dark brown, Liquid

Molecular weight: 158.22

Ref: 02-L03541

1-Naphthalenemethylamine

CAS: 118-31-0

Formula: C₁₁H₁₁N

Purity: 95%

Color and Shape: Liquid

Molecular weight: 157.2117

Ref: IN-DA0032TG

1-Naphthylmethylamine

CAS: 118-31-0

Formula: C₁₁H₁₁N

Molecular weight: 157.22

Ref: 7W-GK8332

1-Naphthylmethylamine

CAS: 118-31-0

Formula: C₁₁H₁₁N

Purity: >98.0%(GC)(T)

Color and Shape: Colorless to Light yellow clear liquid

Molecular weight: 157.22

Ref: 3B-N1042

1-(Aminomethyl)naphthalene

CAS: 118-31-0

1-(Aminomethyl)naphthalene

Formula: C₁₁H₁₁N

Purity: 98%

Color and Shape: brown liquid

Molecular weight: 157.21g/mol

Ref: 54-OR40514

1-Naphthalenemethylamine

CAS: 118-31-0

Formula: C₁₁H₁₁N

Purity: 95%

Color and Shape: Liquid

Molecular weight: 157.216

Ref: 10-F092602

1-(Aminomethyl)naphthalene

CAS: 118-31-0

1-(Aminomethyl)naphthalene is a hydrogen bond-forming molecule that has high values of hydrochloric acid. This compound reacts with sodium carbonate to form glycoside derivatives, which have been shown to display light emission. 1-(Aminomethyl)naphthalene can be used in the synthesis of oxytocin and toll-like receptor ligands, as well as other chemical reactions. The carbonyl group found in this molecule is responsible for the reactivity and stability of this compound.

Formula: C₁₀H₇CH₂NH₂

Purity: Min. 95%

Color and Shape: Clear Colourless To Yellow Liquid

Molecular weight: 157.21 g/mol

Ref: 3D-FA12539