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Home > Encyclopedia > 5-Methoxy-N,N-dimethyl-1H-indole-3-methanamine

5-Methoxy-N,N-dimethyl-1H-indole-3-methanamine

5-Methoxy-N,N-dimethyl-1H-indole-3-methanamine structure

5-Methoxy-N,N-dimethyl-1H-indole-3-methanamine 

structure
  • CAS No:

    16620-52-3

  • Formula:

    C12H16N2O

  • Chemical Name:

    5-Methoxy-N,N-dimethyl-1H-indole-3-methanamine

  • Synonyms:

    1H-Indole-3-methanamine,5-methoxy-N,N-dimethyl-;Indole,3-[(dimethylamino)methyl]-5-methoxy-;5-Methoxy-N,N-dimethyl-1H-indole-3-methanamine;5-Methoxygramine;NSC 88885;3-Dimethylaminomethyl-5-methoxyindole;5-Methoxy-3-(dimethylaminomethyl)indole;[(5-Methoxy-1H-indol-3-yl)methyl]dimethylamine;1-(5-Methoxy-1H-indol-3-yl)-N,N-dimethylmethanamine

5-Methoxy-N,N-dimethyl-1H-indole-3-methanamine Basic Attributes

204.27

204.27

240-669-8

J6ZN008RY8

88885

DTXSID30168081

2933990090

Characteristics

28.26000

2.23810

white to almost white crystalline powder

1.0565

127.5-128.0 °C @ Solvent: Ethanol

342.77°C (rough estimate)

156.2ºC

1.6000 (estimate)

Refrigerator (+4ºC)

0.000126mmHg at 25°C

16.70±0.30

Safety Information

3

34-22

22-24/25

NL7700000

C,Xi

|Danger|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P260, P264, P270, P280, P301+P312, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P330, P363, P405, and P501|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

Drug Information

methoxygramine

5-Methoxy-N,N-dimethyl-1H-indole-3-methanamine Use and Manufacturing

• ;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

Computed Properties

Molecular Weight:204.27
XLogP3:1.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:204.126263138
Monoisotopic Mass:204.126263138
Topological Polar Surface Area:28.3
Heavy Atom Count:15
Complexity:208
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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