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

Description

N-PHENYL-1,2,3,4-TETRAHYDRO-2-AMINONAPHTHALENE, with the molecular formula C16H17N, is a colorless to light yellow liquid chemical compound. It is characterized by a strong, musky odor and is widely recognized for its use as a fragrance ingredient in the perfumery and personal care industries. N-PHENYL-1,2,3,4-TETRAHYDRO-2-AMINONAPHTHALENE also serves as a crucial raw material in the synthesis of various organic compounds, contributing to its versatility in chemical applications.

Uses

Used in Perfumery and Personal Care Industry:
N-PHENYL-1,2,3,4-TETRAHYDRO-2-AMINONAPHTHALENE is used as a fragrance ingredient for its distinct musky scent, adding depth and richness to perfumes and personal care products. Its strong odor profile makes it a valuable component in creating long-lasting and complex fragrances.
Used in Organic Synthesis:
In the realm of organic chemistry, N-PHENYL-1,2,3,4-TETRAHYDRO-2-AMINONAPHTHALENE is utilized as a raw material in the synthesis of a variety of organic compounds. Its structural properties allow it to be a key intermediate in the production of different chemical entities, enhancing its importance in chemical manufacturing processes.
Safety and Storage:
It is essential to handle N-PHENYL-1,2,3,4-TETRAHYDRO-2-AMINONAPHTHALENE with care due to its potential to cause skin and eye irritation. Proper safety measures should be taken during its use, including the use of protective equipment. Additionally, it should be stored in a cool, dry place, away from heat and open flames to prevent any hazardous incidents.

Upstream product

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

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