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16712-55-3

3-Methoxy-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 16712-55-3 Structure

  • Basic information

    1. Product Name: 3-Methoxy-1H-indole
    2. Synonyms: 3-Methoxy-1H-indole
    3. CAS NO:16712-55-3
    4. Molecular Formula: C9H9NO
    5. Molecular Weight: 147.17386
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 16712-55-3.mol

  • Chemical Properties

    1. Melting Point: 69 °C
    2. Boiling Point: 138-140 °C(Press: 3-4 Torr)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.169±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 16.49±0.30(Predicted)
    10. CAS DataBase Reference: 3-Methoxy-1H-indole(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-Methoxy-1H-indole(16712-55-3)
    12. EPA Substance Registry System: 3-Methoxy-1H-indole(16712-55-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 16712-55-3(Hazardous Substances Data)

16712-55-3 Usage

Derivative

Indole derivative

Functional Group

Methoxy group ( \textCH3\textO) attached to the carbon 3 position of the indole ring

Usage

Organic Synthesis: Commonly used as a building block in organic synthesis
Pharmaceutical Research: Used in pharmaceutical research for drug development

Pharmacological Properties

Serotonin Reuptake Inhibition: Investigated for its potential as a serotonin reuptake inhibitor

Research Significance

Drug Synthesis: Investigated for its potential in the synthesis of various drug molecules

Scientific Interest

Research Studies: Shown promise in various research studies
Continued Interest: Continues to be of interest in the scientific community

Check Digit Verification of cas no

The CAS Registry Mumber 16712-55-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,1 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16712-55:
(7*1)+(6*6)+(5*7)+(4*1)+(3*2)+(2*5)+(1*5)=103
103 % 10 = 3
So 16712-55-3 is a valid CAS Registry Number.

16712-55-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Methoxy-1H-indole

1.2 Other means of identification

Product number -
Other names 3-methoxy-indole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:16712-55-3 SDS

16712-55-3Relevant articles and documents

INTRODUCTION OF NUCLEOPHILES OR ETHYL GROUP TO THE INDOLE NUCLEUS THROUGH NUCLEOPHILIC SUBSTITUTION AND/OR RADICAL REACTIONS OF 1-METHOXYINDOLE-3- AND -2-CARBOXALDEHYDE

Yamada, Fumio,Fukui, Yoshikazu,Shinmyo, Daisuke,Somei, Masanori

, p. 99 - 104 (2007/10/02)

1-Methoxyindole-3- and -2-carboxaldehyde were found to undergo nucleophilic substitution and radical reactions resulting in the introduction of nucleophiles and/or ethyl group at the 2- or 3-position.

PREPARATION OF 1-HYDROXYINDOLE DERIVATIVES AND A NEW ROUTE TO 2-SUBSTITUTED INDOLES

Kawasaki, Toshiya,Kodama, Atsushi,Nishida, Tokiko,Shimizu, Kazuhisa,Somei, Masanori

, p. 221 - 227 (2007/10/02)

An easy handling method of 1-hydroxyindole is developed.Based on the method, preparation and reaction of 1-hydroxyindole derivatives are investigated.A new regioselective lithiation of 1-methoxyindole and its application for the synthesis of 2-substituted indoles are also reported.

A NEW CARBON-CARBON BOND FORMING REACTION IN INDOLE CHEMISTRY. C3-ARYLATION AND ALKYLATION WITH PHENYL (β-INDOLYL)IODONIUM TRIFLUOROACETATE

Moriarty, Robert M.,Ku, Y. Y.,Sultana, M.,Tuncay, Atilla

, p. 3071 - 3074 (2007/10/02)

Phenyl(β-indolyl)iodonium trifuoroacetate was reacted with various alkyl and aryllithiums (CH3, n-C4H9, C3H5, C6H5) in BF3Et2O/THF to yield C3-alkylation and arylation of the indole nucleus with reductive elimination of iodobenzene.

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