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5-METHOXYGRAMINE

5-METHOXYGRAMINE Structure
5-METHOXYGRAMINE
  • CAS No.16620-52-3
  • Chemical Name:5-METHOXYGRAMINE
  • CBNumber:CB5245525
  • Molecular Formula:C12H16N2O
  • Formula Weight:204.27
  • MOL File:16620-52-3.mol
5-METHOXYGRAMINE Property
  • Melting point 123-126 °C (lit.)
  • Boiling point 342.77°C (rough estimate)
  • Density 1.0565 (rough estimate)
  • refractive index 1.6000 (estimate)
  • storage temp. Refrigerator (+4°C)
  • pka 16.70±0.30(Predicted)
  • BRN 170533
  • CAS DataBase Reference 16620-52-3(CAS DataBase Reference)
  • FDA UNII J6ZN008RY8
  • UNSPSC Code 12352100
  • NACRES NA.22
Safety
  • Hazard Codes  :C,Xi
  • Risk Statements  :34-22
  • Safety Statements  :22-24/25
  • WGK Germany  :3
  • RTECS  :NL7700000
  • F  :10
  • HS Code  :29339900
  • Toxicity :mouse,LD50,intraperitoneal,130mg/kg (130mg/kg),Psychopharmacologia Vol. 16, Pg. 385, 1970.
Hazard and Precautionary Statements (GHS)
  • Symbol(GHS)
  • Signal wordDanger
  • Hazard statements H302-H314
  • Precautionary statements P264-P270-P301+P312-P330-P501-P260-P264-P280-P301+P330+P331-P303+P361+P353-P363-P304+P340-P310-P321-P305+P351+P338-P405-P501
5-METHOXYGRAMINE Price More Price(1)
  • Brand: Sigma-Aldrich(India)
  • Product number: M14870
  • Product name : 5-Methoxygramine
  • Purity: 99%
  • Packaging: 5G
  • Price: ₹13087.43
  • Updated: 2022/06/14
  • Buy: Buy

5-METHOXYGRAMINE Chemical Properties,Usage,Production

  • Chemical Properties white to almost white crystalline powder
  • Uses
    • Reactant for preparation of dopamine D2 receptor antagonists
    • Reactant for asymmetric preparation of ethenyl(tetrahydro)carbazoledicarboxylates via gold(I)-catalyzed intramolecular Friedel-Crafts allylic alkylation reaction
    • Reactant for preparation of N-substituted 3-aryl-8-azabicyclo[3.2.1]octan-3-ols as dopamine D2-like receptor ligands
    • Reactant for preparation of substituted N-trimethoxybenzoyl indoles, indolines, and a tetrahydroquinoline via N-aroylation with trimethoxybenzoyl chloride or anhydride as antitubulin agents
    • Reactant for preparation of indolylmethanesulfonamide and its methoxy derivatives
  • Uses • ;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 in
5-METHOXYGRAMINE Preparation Products And Raw materials
Raw materials
Preparation Products
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5-METHOXYGRAMINE Spectrum
16620-52-3, 5-METHOXYGRAMINERelated Search:
  • Indoles and derivatives
  • Heterocyclic Compounds
  • Indoline & Oxindole
  • Indoles
  • Heterocyclic Building Blocks
  • Chemical Synthesis
  • C12
  • Building Blocks
  • 高端化学
  • Building Blocks
  • Indoles
  • Heterocyclic Building Blocks
  • 1-(5-甲氧基-1H-吲哚-3-基)-N,N-二甲基甲胺
  • 5-甲氧基-N,N-二甲基-1H-吲哚-3-甲醇
  • 5-甲氧基-3-二甲胺基甲基吲哚
  • 3-二甲基胺甲基-5-甲氧基吲哚
  • 5-甲氧基芦竹碱
  • 16620-52-3
  • (5-methoxy-1H-indol-3-yl)methyl-dimethylammonium
  • 1H-Indole-3-methanamine, 5-methoxy-N,N-dimethyl-
  • N-[(5-METHOXY-1H-INDOL-3-YL)METHYL]-N,N-DIMETHYLAMINE
  • 2-dimethylaminomethyl-5-methoxyindole
  • 5-METHOXYGRAMINE
  • (5-METHOXY-1H-INDOL-3-YLMETHYL)-DIMETHYL-AMINE
  • 3-(DIMETHYLAMINOMETHYL)-5-METHOXY-INDOLE
  • 3-[(Dimethylamino)methyl]-5-methoxy-1H-indole
  • TIMTEC-BB SBB003509
  • 5-methoxy-n,n-dimethyl-1h-indole-3-methanamin
  • 5-methoxy-3-(dimethylaminomethyl)indole
  • 3-((dimethylamino)methyl)-5-methoxy-indol
  • NSC 88885
  • 5-Methoxygramine,99%
  • 3-ETHYL-1H-PYRAZOL-5-AMINE HCL
  • 5-Methoxygramine or 5-Methoxy-3-(Dimethylaminomethyl)-indole
  • methoxygramine
  • 5-Methoxygramine, N,N-Dimethyl-(5-methoxy-1H-indol-3-yl)methylamine
  • 5-METHOXYGRAMINE 99%