33816-55-6

Basic information

• Product Name: N-PHENYL-1,2,3,4-TETRAHYDRO-2-AMINONAPHTHALENE
• Synonyms: 2-Naphthylamine,1,2,3,4-tetrahydro-N-phenyl- (8CI); N-Phenyl-1,2,3,4-tetrahydro-2-naphthylamine
• CAS NO: 33816-55-6
• Molecular Formula: C₁₆H₁₇N
• Molecular Weight: 223.31
• Mol File: 33816-55-6.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-PHENYL-1,2,3,4-TETRAHYDRO-2-AMINONAPHTHALENE(CAS DataBase Reference)
• NIST Chemistry Reference: N-PHENYL-1,2,3,4-TETRAHYDRO-2-AMINONAPHTHALENE(33816-55-6)
• EPA Substance Registry System: N-PHENYL-1,2,3,4-TETRAHYDRO-2-AMINONAPHTHALENE(33816-55-6)

Safety Data

• Hazardous Substances Data: 33816-55-6(Hazardous Substances Data)

Usage

General Description

N-PHENYL-1,2,3,4-TETRAHYDRO-2-AMINONAPHTHALENE is a chemical compound with the molecular formula C16H17N. It is a colorless to light yellow liquid that is used as a fragrance ingredient in perfumes and personal care products. It has a strong, musky odor and is commonly used in the production of musk fragrances. N-PHENYL-1,2,3,4-TETRAHYDRO-2-AMINONAPHTHALENE is also used as a raw material in the synthesis of various organic compounds. It is important to handle this chemical with care as it may cause skin and eye irritation, and it should be stored in a cool, dry place away from heat and flames.

Upstream product

• 135-88-6 N-Phenyl-2-naphthylamine 
• 530-93-8 1,2,3,4-tetrahydronaphthalen-2-one 
• 62-53-3 aniline 
• 59648-41-8 2-(phenylamino)-3,4-dihydronaphthalen-1(H)-one 
• 530-91-6 1,2,3,4-tetrahydronaphthalen-2 ol 

Downstream Products

• 52802-21-8 N-phenyl-1,2,3,4-tetrahydro-2-aminonaphthalene 
• 1002354-11-1 N-(2-tetralyl)-N-phenyl-2-chloroacetamide 
• 52802-42-3 2-[N-phenyl-N-(β-chloropropionyl)]-amino-(1,2,3,4-tetrahydronaphthalene) 

Relevant articles and documents

Use of (cyclopentadienone)iron tricarbonyl complexes for c-n bond formation reactions between amines and alcohols

The application of a series of (cyclopentadienone)iron tricarbonyl complexes to "borrowing hydrogen" reactions between amines and alcohols was completed in order to assess their catalytic activity. The electronic variation of the aromatic groups flanking the C?O of the cyclopentadienone influenced the efficiency of the reactions; however, in other cases, the Kn?lker catalyst 1, containing trimethylsilyl groups flanking the cyclopentadienone ketone, gave the best results. In some cases, the change of the ratio of amine to alcohol improves the conversion significantly. The application of iron catalysts to the synthesis of a range of amines, including unsaturated amines, was investigated.

DERMAL ANESTHETIC COMPOUNDS

The present invention relates to new tetralin compounds, the methods of preparing said tetralin compounds, the method of using said tetralin compounds as local anesthetics and dermal anesthetics, said compounds having particularly valuable properties as d