5-Methoxygramine

• Catalog No.: M14870
• CAS Number: 16620-52-3
• M. F.: C12H16N2O
• M. W.: 204.26824
• Purity: 99%

SYNONYMS

• Title: 5-甲氧基芦竹碱
• IUPAC name: [(5-methoxy-1H-indol-3-yl)methyl]dimethylamine
• IUPAC Traditional name: methoxygramine
• Synonyms: NSC 88885; 5-甲氧基-3-二甲胺基甲基吲哚; 3-(Dimethylaminomethyl)-5-methoxyindole

DATABASE IDS

• EC Number: 240-669-8
• Beilstein Number: 170533
• CAS Number: 16620-52-3
• PubChem SID: 24896649
• MDL Number: MFCD00005630

PROPERTIES

• Empirical Formula (Hill Notation): C12H16N2O
• Purity: 99%
• Melting Point: 123-126 °C(lit.)
• Personal Protective Equipment: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• RTECS: NL7700000
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1, 5 g in glass bottle
Application

• Reactant for preparation of dopamine D2 receptor antagonists1
• Reactant for asymmetric preparation of ethenyl(tetrahydro)carbazoledicarboxylates via gold(I)-catalyzed intramolecular Friedel-Crafts allylic alkylation reaction2
• Reactant for preparation of N-substituted 3-aryl-8-azabicyclo[3.2.1]octan-3-ols as dopamine D2-like receptor ligands3
• Reactant for preparation of substituted N-trimethoxybenzoyl indoles, indolines, and a tetrahydroquinoline via N-aroylation with trimethoxybenzoyl chloride or anhydride as antitubulin agents4
• Reactant for preparation of indolylmethanesulfonamide and its methoxy derivatives5

Description (简体中文)

包装
1, 5 g in glass bottle
Application

• Reactant for preparation of dopamine D2 receptor antagonists1
• Reactant for asymmetric preparation of ethenyl(tetrahydro)carbazoledicarboxylates via gold(I)-catalyzed intramolecular Friedel-Crafts allylic alkylation reaction2
• Reactant for preparation of N-substituted 3-aryl-8-azabicyclo[3.2.1]octan-3-ols as dopamine D2-like receptor ligands3
• Reactant for preparation of substituted N-trimethoxybenzoyl indoles, indolines, and a tetrahydroquinoline via N-aroylation with trimethoxybenzoyl chloride or anhydride as antitubulin agents4
• Reactant for preparation of indolylmethanesulfonamide and its methoxy derivatives5