1-Methylindole

1-Methylindole Basic information
Product Name:1-Methylindole
Synonyms:1-METHYLINDOLE (N-);1-METHYLINDOLE;1-METHYLINDOL;1H-Indole, 1-methyl-;L-Methylindole;1-METHYLINDOLE, 97+%;N-Methyindole;1-Methylindol, 98+%
CAS:603-76-9
MF:C9H9N
MW:131.17
EINECS:210-057-5
Product Categories:Heterocycle-Indole series;Simple Indoles;blocks;Indoles;Building Blocks;Heterocyclic Building Blocks;IndolesOxindoles;Indole;bc0001
Mol File:603-76-9.mol
1-Methylindole Structure
1-Methylindole Chemical Properties
Melting point 61.2°C (estimate)
Boiling point 133 °C26 mm Hg(lit.)
density 1.051 g/mL at 20 °C(lit.)
refractive index n20/D 1.606(lit.)
Fp >230 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform (Soluble), DMSO (Slightly)
form Liquid, May Develop Some Turbidity or Precipitate
color Colorless to white
Water Solubility insoluble
Sensitive Light Sensitive
BRN 111026
Stability:Light sensitive. Combustible. Incompatible with strong oxidizing agents.
InChIKeyBLRHMMGNCXNXJL-UHFFFAOYSA-N
LogP2.720
CAS DataBase Reference603-76-9(CAS DataBase Reference)
NIST Chemistry Reference1H-Indole, 1-methyl-(603-76-9)
EPA Substance Registry System1H-Indole, 1-methyl- (603-76-9)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 22-24/25-37/39-26
RIDADR UN 3334
WGK Germany 3
13
TSCA Yes
HS Code 29339990
MSDS Information
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1-Methylindole English
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1-Methylindole Usage And Synthesis
Chemical Propertiesdeep yellow viscous liquid with a very unpleasant smell
Uses1-Methylindole is useful for the determination of association constant for the electron-donor-acceptor complexes with 1-(2,4,6-trinitrophenyl) propan-2-one. It acts as a reactant for the preparation of polycyclic derivatives of indoles, bisindole derivatives and pharmaceutically active 2-oxo-1-pyrrolidine analogues. It is also used as a reactant for the preparation of Positron Emission Tomography (PET) imaging agents of protein kinase C (PKC) and glycogen synthase kinase-3 (GSK-3).
Synthesis Reference(s)Synthetic Communications, 26, p. 1349, 1996 DOI: 10.1080/00397919608003495
Tetrahedron Letters, 27, p. 377, 1986 DOI: 10.1016/S0040-4039(00)84023-X
General Description1-Methylindole undergoes Au(III)/TPPMS-catalyzed benzylation reaction with benzhydryl and benzylic alcohols.
1-Methylindole Preparation Products And Raw materials
Preparation ProductsN-(4-fluoro-2-Methoxy-5-nitrophenyl)-4-(1-Methylindol-3-yl)pyriMidin-2-aMine-->RAMOSETRON-->AZ 7550-->1-(1-METHYL-1H-INDOL-3-YL)-1-ETHANONE-->1-METHYL-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1H-INDOLE-->N-Isopropylacetamide-->1-METHYL-2-INDOLINONE-->1-METHYLTRYPTAMINE-->1-Methylindole-3-carboxaldehyde
9-Vinylcarbazole 1-Methylindole-3-carboxaldehyde 1-Methylindole 2-Methylindole 1-Methylindole-2-carboxylic acid 1-METHYL-DL-TRYPTOPHAN BASIC RED 29 3-Amino-9-ethylcarbazole N-METHYLCARBAZOLE 1,2-Dimethylindole N-PHENYLCARBAZOLE HYDROCHLORIDE 1,4,5,8,9-PENTAMETHYLCARBAZOLE 5-BROMOINDOXYL DIACETATE 1-Methyl-2-phenylindole N-Ethylcarbazole 9-Ethyl-3-nitrocarbazole 1,3-DIACETOXYINDOLE CARBAZOL-9-YL-METHANOL

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