| Identification | More | [Name]
5-METHOXYGRAMINE | [CAS]
16620-52-3 | [Synonyms]
3-(DIMETHYLAMINOMETHYL)-5-METHOXY-INDOLE
(5-METHOXY-1H-INDOL-3-YLMETHYL)-DIMETHYL-AMINE
5-METHOXYGRAMINE
N-[(5-METHOXY-1H-INDOL-3-YL)METHYL]-N,N-DIMETHYLAMINE
TIMTEC-BB SBB003509
3-((dimethylamino)methyl)-5-methoxy-indol
5-methoxy-3-(dimethylaminomethyl)indole
5-methoxy-n,n-dimethyl-1h-indole-3-methanamin
2-dimethylaminomethyl-5-methoxyindole
3-[(Dimethylamino)methyl]-5-methoxy-1H-indole
5-Methoxygramine, N,N-Dimethyl-(5-methoxy-1H-indol-3-yl)methylamine
methoxygramine
5-Methoxygramine or 5-Methoxy-3-(Dimethylaminomethyl)-indole
5-METHOXYGRAMINE 99%
3-ETHYL-1H-PYRAZOL-5-AMINE HCL | [EINECS(EC#)]
240-669-8 | [Molecular Formula]
C12H16N2O | [MDL Number]
MFCD00005630 | [Molecular Weight]
204.27 | [MOL File]
16620-52-3.mol |
| Chemical Properties | Back Directory | [Appearance]
white to almost white crystalline powder | [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) | [Detection Methods]
HPLC | [BRN ]
170533 | [CAS DataBase Reference]
16620-52-3(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
C,Xi | [Risk Statements ]
R34:Causes burns.
R22:Harmful if swallowed. | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [RTECS ]
NL7700000
| [F ]
10 | [HS Code ]
29339900 |
| Hazard Information | Back Directory | [Chemical Properties]
white to almost white crystalline powder | [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 | [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
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Sigma-Aldrich
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