123048-17-9

Basic information

• Product Name: Phyltetralin
• Synonyms: Phyltetralin;(1R,2S,3S)-1-(3,4-Dimethoxyphenyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-2,3-bis(methoxymethyl)naphthalene
• CAS NO: 123048-17-9
• Molecular Formula: C₂₄H₃₂O₆
• Molecular Weight: 416.50728
• Mol File: 123048-17-9.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Phyltetralin(CAS DataBase Reference)
• NIST Chemistry Reference: Phyltetralin(123048-17-9)
• EPA Substance Registry System: Phyltetralin(123048-17-9)

Safety Data

• Hazardous Substances Data: 123048-17-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
Phyltetralin is used as a starting material for the synthesis of various pharmaceutical compounds. Its aromatic nature and chemical reactivity make it suitable for the development of new drugs and medications.
Used in Fragrance Industry:
Phyltetralin is used as a solvent in the production of fragrances. Its sweet, floral odor contributes to the creation of various scent profiles in perfumes and other scented products.
Used in Dye Manufacturing:
Phyltetralin is used in the manufacturing of dyes due to its chemical properties, which allow for the development of a wide range of colorants for various applications.
Used in Pesticide Production:
Phyltetralin serves as a starting material in the production of pesticides, where its chemical structure can be modified to create effective and targeted pest control agents.
Used in Chemical Product Manufacturing:
Phyltetralin is utilized in the manufacturing of various chemical products, including solvents, due to its versatile chemical properties and its ability to act as a starting material for the synthesis of other compounds.

Upstream product

• 66510-81-4 (+)-dimethyl-β-conidendryl alcohol 
• 74-88-4 methyl iodide 
• 61248-24-6 r-1-(3,4-dimethoxyphenyl)-t-2,c-3-bis(hydroxymethyl)-6,7-dimethoxy-1,2,3,4-tetrahydronaphthalene 
• 54370-00-2 2-bromo-4,5-dimethoxybenzyl alcohol 
• 82837-97-6 dimethyl trans(1,2),trans(2,3)-6,7-dimethoxy-1-(3,4-dimethoxyphenyl)-1,3,4-tetrahydronaphthalene-2,3-dicarboxylate 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 82792-82-3 1-(3,4-Dimethoxy-phenyl)-5,6-dimethoxy-1,3-dihydro-benzo[c]thiophene 2,2-dioxide 
• 82792-88-9 (2-bromo-4,5-dimethoxyphenyl)methanethiol 
• 82792-86-7 1-(3,4-Dimethoxy-phenyl)-5,6-dimethoxy-1,3-dihydro-benzo[c]thiophene 
• 82792-84-5 (3,4-Dimethoxy-phenyl)-(2-hydroxymethyl-4,5-dimethoxy-phenyl)-methanol 
• 79150-37-1 2,3-Dimethoxy-7-methyl-naphthalin-6-carbonsaeure-ethylester 
• 114839-29-1 2-(ethoxycarbonyl)-3-(bromomethyl)-6,7-dimethoxynaphthalene 
• 114839-34-8 (4R,5R)-2-[(1R,2S)-1-(3,4-Dimethoxy-phenyl)-6,7-dimethoxy-3-methoxymethyl-1,2-dihydro-naphthalen-2-yl]-4-methoxymethyl-5-methyl-4,5-dihydro-oxazole 
• 114839-36-0 (1R,2S)-1-(3,4-Dimethoxy-phenyl)-6,7-dimethoxy-3-methoxymethyl-1,2-dihydro-naphthalene-2-carboxylic acid (1S,2S)-2-amino-3-methoxy-1-methyl-propyl ester; compound with trifluoro-acetic acid 

Relevant articles and documents

Asymmetric radical synthesis of 2,5-diaryl-2,3-dihydrofurans - Application to the preparation of (+)-phyltetralin

The diastereoselective MnIII-promoted radical addition of βoxo ester 1 onto N-cinnamoyloxazolidinone 2 affords, after removal of the chiral auxiliary, the enantiopure 2,5-diaryl2,3-dihydrofuran (-)-4. Its SnCl4-induced rearrangement

The Synthesis of Lignans and Related Structures using Quinodimethanes and Isobenzofurans: Approaches to the Podophyllins

Novel routes to 1-aryl-5,6-dialkoxy-1,3-dihydrobenzothiophene 2,2-dioxides (13) and to the corresponding benzofuran (8) have been developed; these species yield quinodimethanes (12) via thermal extrusion of SO2 and isobenzofurans (5c) in an acid-cat

The Preparation of Lignans via Intermolecular Cycloadditions with Quinodimethanes

Certain lignans can be prepared using, as the key step, a thermal reaction between 1-(aryl)-1,3-dihydro-5,6-dialkoxy-benzothiophen 2,2-dioxides and dienophiles.

Synthesis of Aryltetralin and Dibenzylbutyrolactone Lignans: (+/-)-Lintetralin, (+/-)-Phyltetralin, and (+/-)-Kusunokinin

Application of a general synthetic pathway for aryltetralin and dibenzylbutyrolactone lignans, starting from the lithium enolate of 3-(3,4-dimethoxybenzyl)butyrolactone (1) led to syntheses of (+/-)-lintetralin (4), (+/-)-phyltetralin (5), (+/-)-isogalcat

STRUCTURE AND SYNTHESYS OF HYPOPHYLLANTHIN, NIRTETRALIN, PHYLTETRALIN AND LINTETRALIN

Structures propounded for the four aryltetralin lignan constituents isolated from Phyllanthus niruri Linn. are confirmed by syntheses of their (+/-)-forms.