CAS 14430-23-0|5,6-Dimethoxyindole

Introduction：Basic information about CAS 14430-23-0|5,6-Dimethoxyindole, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. Chemical & Physical Properties
3. Safety Information
4. Customs
5. Articles3
6. Synonyms

Common Name	5,6-Dimethoxyindole
CAS Number	14430-23-0	Molecular Weight	177.200
Density	1.2±0.1 g/cm3	Boiling Point	320.3±22.0 °C at 760 mmHg
Molecular Formula	C₁₀H₁₁NO₂	Melting Point	154-157 °C(lit.)
MSDS	USA	Flash Point	117.4±12.6 °C

Names

Name	5,6-dimethoxyindole
Synonym	More Synonyms

Chemical & Physical Properties

Density	1.2±0.1 g/cm3
Boiling Point	320.3±22.0 °C at 760 mmHg
Melting Point	154-157 °C(lit.)
Molecular Formula	C₁₀H₁₁NO₂
Molecular Weight	177.200
Flash Point	117.4±12.6 °C
Exact Mass	177.078979
PSA	34.25000
LogP	1.82
Vapour Pressure	0.0±0.7 mmHg at 25°C
Index of Refraction	1.609
InChIKey	QODBZRNBPUPLEZ-UHFFFAOYSA-N
SMILES	COc1cc2cc[nH]c2cc1OC

Safety Information

Personal Protective Equipment	Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes	Xi: Irritant;
Safety Phrases	S22-S24/25
RIDADR	NONH for all modes of transport
WGK Germany	3
HS Code	2933990090

Customs

HS Code	2933990090
Summary	2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles3

[Monoamine oxidase inhibitors. I. Synthesis of N-cyclopropyltryptamines].

Farmaco. Sci. 35(9) , 785-90, (1980)

The synthesis of two new N-cyclopropyltryptamines is described. By treating 5,6-dimethoxyindole with oxalyl chloride and N-benzylcyclopropylamine, N-benzyl-N-cyclopropyl-5,6-dimethoxyindole-3-glyoxala...

Cross-polarization dynamics and spin diffusion in some aromatic compounds.

Solid State Nucl. Magn. Reson. 3(3) , 121-35, (1994)

The inversion-recovery cross-polarization (IRCP) magic-angle spinning experiment has been applied to study the 13C-1H cross-polarization dynamics of protonated aromatic carbons in ferrocene, 5,6-dimet...

Structural characterization of two isomeric dimethoxyindoles of biological interest, using high- and low-energy collisional spectroscopy.

Rapid Commun. Mass Spectrom. 3(12) , 413-6, (1989)

It is not possible to distinguish isomers of biologically important dimethoxyindoles using electron-ionization mass spectra, but they may be distinguished by collisionally activated dissociation. In p...

Synonyms

1H-Indole, 5,6-dimethoxy-

5,6-Dimethoxyindole

MFCD00005675

5,6-Dimethoxy-1H-indole

EINECS 238-402-5

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