5-METHOXYINDOLE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C9H9NO
Molecular Weight	147.1739
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

SMILES

COC1=CC2=C(NC=C2)C=C1

InChI

InChIKey=DWAQDRSOVMLGRQ-UHFFFAOYSA-N

InChI=1S/C9H9NO/c1-11-8-2-3-9-7(6-8)4-5-10-9/h2-6,10H,1H3

HIDE SMILES / InChI

Approval Year

PubMed

Show entries

Title	Date	PubMed
A simple procedure for synthesis of roxindole, a dopamine D2-receptor agonist.	2001 Jul	11512277
Indole ring oxidation by activated leukocytes prevents the production of hypochlorous acid.	2005 Nov	16258625
Mechanism for the direct synthesis of tryptophan from indole and serine: a useful NMR technique for the detection of a reactive intermediate in the reaction mixture.	2010 Oct	20799376

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Patents

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Name

Type

Language

5-METHOXYINDOLE

Systematic Name

English

INDOLE, 5-METHOXY-

Systematic Name

English

INDOL-5-YL METHYL ETHER

Systematic Name

English

NSC-521752

Code

English

5-METHOXY-1H-INDOLE

Systematic Name

English

Showing 1 to 5 of 7 entries

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Code System

Code

Type

Description

EPA CompTox

DTXSID80143424

PRIMARY

CAS

1006-94-6

PRIMARY

FDA UNII

DQM3AS43PQ

PRIMARY

NSC

521752

PRIMARY

PUBCHEM

13872

PRIMARY

Showing 1 to 5 of 6 entries

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SUBSTANCE RECORD


					DQM3AS43PQ

5-METHOXYINDOLE