3-O-METHYLDOPAMINE

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C9H13NO2
Molecular Weight	167.205
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of 3-O-METHYLDOPAMINE

Structure Search

SMILES

COC1=CC(CCN)=CC=C1O

InChI

InChIKey=DIVQKHQLANKJQO-UHFFFAOYSA-N

InChI=1S/C9H13NO2/c1-12-9-6-7(4-5-10)2-3-8(9)11/h2-3,6,11H,4-5,10H2,1H3

HIDE SMILES / InChI

Molecular Formula	C9H13NO2
Molecular Weight	167.205
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

Substance Class	Chemical Created by `admin` on `Sat Dec 16 18:54:30 UTC 2023` Edited by `admin` on `Sat Dec 16 18:54:30 UTC 2023`
Record UNII	JCH2767EDP
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

3-O-METHYLDOPAMINE

Systematic Name

English

4-(2-AMINOETHYL)-2-METHOXYPHENOL

Systematic Name

English

4-HYDROXY-3-METHOXY-.BETA.-PHENETHYLAMINE

Systematic Name

English

DOPAMINE HYDROCHLORIDE IMPURITY B [EP IMPURITY]

Common Name

English

4-HYDROXY-3-METHOXYPHENYLETHYLAMINE

Systematic Name

English

PHENOL, 4-(2-AMINOETHYL)-2-METHOXY-

Systematic Name

English

HOMOVANILLINAMINE

Common Name

English

HYDROXY-3-METHOXYPHENETHYLAMINE, 4-

Systematic Name

English

2-METHOXY-4-(2-AMINOETHYL)PHENOL

Systematic Name

English

4-HYDROXY-3-METHOXY-2-PHENETHYLAMINE

Systematic Name

English

3-METHOXY-P-TYRAMINE

Common Name

English

3-METHOXYTYRAMINE

Systematic Name

English

GUAIACOL, 4-(2-AMINOETHYL)-

Systematic Name

English

2-(4-HYDROXY-3-METHOXYPHENYL)ETHYLAMINE

Systematic Name

English

4-HYDROXY-3-METHOXYPHENETHYLAMINE

Systematic Name

English

HOMOVANILLYLAMINE

Systematic Name

English

DOPAMINE IMPURITY B [EP IMPURITY]

Common Name

English

Classification Tree Code System Code

LOINC

80156-3

Created by admin on Sat Dec 16 18:54:30 UTC 2023 , Edited by admin on Sat Dec 16 18:54:30 UTC 2023

LOINC

40409-5

Created by admin on Sat Dec 16 18:54:30 UTC 2023 , Edited by admin on Sat Dec 16 18:54:30 UTC 2023

LOINC

54343-9

Created by admin on Sat Dec 16 18:54:30 UTC 2023 , Edited by admin on Sat Dec 16 18:54:30 UTC 2023

LOINC

50140-3

Created by admin on Sat Dec 16 18:54:30 UTC 2023 , Edited by admin on Sat Dec 16 18:54:30 UTC 2023

LOINC

50139-5

Created by admin on Sat Dec 16 18:54:30 UTC 2023 , Edited by admin on Sat Dec 16 18:54:30 UTC 2023

LOINC

48381-8

Created by admin on Sat Dec 16 18:54:30 UTC 2023 , Edited by admin on Sat Dec 16 18:54:30 UTC 2023

LOINC

54344-7

Created by admin on Sat Dec 16 18:54:30 UTC 2023 , Edited by admin on Sat Dec 16 18:54:30 UTC 2023

LOINC

48380-0

Created by admin on Sat Dec 16 18:54:30 UTC 2023 , Edited by admin on Sat Dec 16 18:54:30 UTC 2023

LOINC

32618-1

Created by admin on Sat Dec 16 18:54:30 UTC 2023 , Edited by admin on Sat Dec 16 18:54:30 UTC 2023

Code System Code Type Description

MESH

C001746

Created by admin on Sat Dec 16 18:54:30 UTC 2023 , Edited by admin on Sat Dec 16 18:54:30 UTC 2023

PRIMARY

PUBCHEM

1669

Created by admin on Sat Dec 16 18:54:30 UTC 2023 , Edited by admin on Sat Dec 16 18:54:30 UTC 2023

PRIMARY

FDA UNII

JCH2767EDP

Created by admin on Sat Dec 16 18:54:30 UTC 2023 , Edited by admin on Sat Dec 16 18:54:30 UTC 2023

PRIMARY

WIKIPEDIA

3-Methoxytyramine

Created by admin on Sat Dec 16 18:54:30 UTC 2023 , Edited by admin on Sat Dec 16 18:54:30 UTC 2023

PRIMARY

CAS

554-52-9

Created by admin on Sat Dec 16 18:54:30 UTC 2023 , Edited by admin on Sat Dec 16 18:54:30 UTC 2023

PRIMARY

RXCUI

1742513

Created by admin on Sat Dec 16 18:54:30 UTC 2023 , Edited by admin on Sat Dec 16 18:54:30 UTC 2023

PRIMARY

EPA CompTox

DTXSID40862189

Created by admin on Sat Dec 16 18:54:30 UTC 2023 , Edited by admin on Sat Dec 16 18:54:30 UTC 2023

PRIMARY

Related Record Type Details


					VTD58H1Z2X

DOPAMINE

PARENT -> METABOLITE INACTIVE

Amount: