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5-Methoxyindole

CAS No.
1006-94-6
Chemical Name:
5-Methoxyindole
Synonyms
5-METHOXY-1H-INDOLE;Methoxyindole 99% indol-5-yl methyl ether;5-methoxy-indol;Femedol;NSC 521752;AKOS JY2082918;5-METHOXYINDOLE;methoxy-5indole;5-MethoxyindoleF;Methoxy-5 indole
CBNumber:
CB4223553
Molecular Formula:
C9H9NO
Molecular Weight:
147.17
MDL Number:
MFCD00005674
MOL File:
1006-94-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-27 08:01:41

5-Methoxyindole Properties

Melting point 52-55 °C (lit.)
Boiling point 176-178 °C/17 mmHg (lit.)
Density 1.1135 (rough estimate)
refractive index 1.5310 (estimate)
Flash point 176-178°C/17mm
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform, Methanol
pka 16.70±0.30(Predicted)
form Crystalline Powder
color White to light brownish
Water Solubility insoluble
Sensitive Light Sensitive
BRN 116722
InChI 1S/C9H9NO/c1-11-8-2-3-9-7(6-8)4-5-10-9/h2-6,10H,1H3
InChIKey DWAQDRSOVMLGRQ-UHFFFAOYSA-N
SMILES COc1ccc2[nH]ccc2c1
CAS DataBase Reference 1006-94-6(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII DQM3AS43PQ
NIST Chemistry Reference 1H-Indole, 5-methoxy-(1006-94-6)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
target organs Respiratory system
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-24/25-37/39
WGK Germany  3
RTECS  NL9500000
8
Hazard Note  Irritant
HazardClass  IRRITANT, KEEP COLD, LIGHT SENSITIVE
HS Code  29339900
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
NFPA 704
1
2 0

5-Methoxyindole price More Price(85)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich M14900 5-Methoxyindole 99% 1006-94-6 1g $28.5 2026-04-30 Buy
Sigma-Aldrich M14900 5-Methoxyindole 99% 1006-94-6 5g $38.8 2026-04-30 Buy
TCI Chemical M0731 5-Methoxyindole >99.0%(GC) 1006-94-6 1g $57 2026-04-30 Buy
TCI Chemical M0731 5-Methoxyindole >99.0%(GC) 1006-94-6 5g $97 2026-04-30 Buy
Usbiological 234279 5-Methoxyindole 99+% (HPLC) ≥99%(HPLC) 1006-94-6 1g $156 2026-06-03 Buy
Product number Packaging Price Buy
M14900 1g $28.5 Buy
M14900 5g $38.8 Buy
M0731 1g $57 Buy
M0731 5g $97 Buy
234279 1g $156 Buy

5-Methoxyindole Chemical Properties, Uses, Production

Chemical Properties

white to light brownish crystalline powder

Uses

5-Methoxyindole (cas# 1006-94-6) is a compound useful in organic synthesis. It can be used to synthesis 1-(Phenylsulfonyl)-5-methoxy-1H-indole.

Preparation

The synthesis of 5-methoxyindole from 5-methoxy-2-oxindole: Conversion of 5-methoxy-2-oxindole to 5-methoxyindole was accomplishedby the chlorination of 5-methoxy-2-oxindole with triphenylphosphine-carbontetrachloride in acetonitrile followed by the catalytic reduction of a chlorine atom in 66% total yield.

Definition

ChEBI: 5-methoxyindole is a member of indoles.

Reactions

5-methoxyindole was treated with sodium hydroxide and phenylsulfonyl chloride in the presence of a catalytic amount of tetrabutylammonium bromide to afford 1-(phenylsulfonyl)indole and 5-methoxy-1-(phenylsufonyl)indole in excellent yields of 100%.

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 26, p. 1405, 1989 DOI: 10.1002/jhet.5570260533
The Journal of Organic Chemistry, 58, p. 5558, 1993 DOI: 10.1021/jo00072a052
Tetrahedron Letters, 27, p. 837, 1986 DOI: 10.1016/S0040-4039(00)84114-3

Synthesis

The synthesis method of 2-pyridinecarboxaldehyde:the three-component coupling reaction of dicarbonyl compounds, aldehydes, and urea/thiourea catalyzed by indium chloride can be efficiently synthesized.

Purification Methods

Crystallise 5-methoxyindole from cyclohexane pet ether or pet ether/Et2O. [Saito & Kikugawa J Heterocycl Chem 16 1325 1979, Beilstein 21 III/IV 765, 21/3 V 18.]

845619-77-4
1006-94-6
Synthesis of 5-Methoxyindole from 1-Propanone, 1-(5-methoxy-1H-indol-1-yl)-2,2-dimethyl-
Global Suppliers ( 621)
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Zhanhua Huibang Chemical Co., Ltd. 13906149256 793211102@qq.com China 152 58
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J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
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INTATRADE GmbH +49 3493/605464 sales@intatrade.de Germany 3563 66
Alfa Aesar 400-6106006 saleschina@alfa-asia.com China 30103 84
TAIYUAN RHF CO.,LTD. +86 351 7031519 sales@RHFChem.com China 2334 56
TCI (Shanghai) Development Co., Ltd. 021-67121386 Sales-CN@TCIchemicals.com China 24512 81
Beijing dtftchem Technology Co., Ltd. 010-60275820 13031183356 elainezt@sina.com China 1386 62
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61

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View Latest Price from 5-Methoxyindole manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
5-Methoxyindole pictures 2026-09-14 5-Methoxyindole
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$129.00-645.00 1g 0.99 25kg Shanghai UCHEM Inc.
5-Methoxyindole pictures 2026-05-28 5-Methoxyindole
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$11.00 1ASSAYS 99% 10000kg Hebei Chuanghai Biotechnology Co,.LTD
5-METHOXYINDOLE pictures 2026-03-20 5-METHOXYINDOLE
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$10.00 1KG 99% 10 mt Hebei Chuanghai Biotechnology Co., Ltd
Methoxyindole 99% indol-5-yl methyl ether 5-Methoxyindole ,98% 5-METHOXYINDOLE (5MeOI) 5-methoxy-1H-indole(SALTDATA: FREE) 5-MethoxyindoleF 5-METHOXYINDOLE REPANIDAL NSC 521752 5-METHOXYINDOLE AKOS JY2082918 RARECHEM AH BS 0117 5-Methoxyindole in stock Factory TIMTEC-BB SBB004094 1H-Indol-5-yl methyl ether 5-methoxy-indol Femedol Indole, 5-methoxy- Methoxy-5 indole methoxy-5indole 5-Methyoxy Indole 5-methyloxyl indole 5-Methoxylindole Methoxyindole,99% Indol-5-yl methyl ether 5-Methoxyindole> 5-Methoxyindole 1006-94-6 5-methoxy-1H-indole - [M2323] 5-METHOXY-1H-INDOLE 1006-94-6 Indoles Simple Indoles Building Blocks Heterocyclic Building Blocks blocks IndolesOxindoles Heterocycles Indoles and derivatives IndoleDerivative Pyrroles & Indoles Heterocyclic Compounds Indole Series Indoles Indoline & Oxindole Indole Building Blocks C7 to C9 Chemical Synthesis Heterocyclic Building Blocks Heterocycle-Indole series Indole Derivatives Simple Indoles Chiral Compound Pyrroles & Indoles Building Blocks Heterocyclic Building Blocks