DOET

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C13H21NO2
Molecular Weight	223.3113
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of DOET

Structure Search

SMILES

CCC1=CC(OC)=C(CC(C)N)C=C1OC

InChI

InChIKey=HXJKWPGVENNMCC-UHFFFAOYSA-N

InChI=1S/C13H21NO2/c1-5-10-7-13(16-4)11(6-9(2)14)8-12(10)15-3/h7-9H,5-6,14H2,1-4H3

HIDE SMILES / InChI

Molecular Formula	C13H21NO2
Molecular Weight	223.3113
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Approval Year

Substance Class	Chemical Created by `admin` on `Sat Dec 16 10:57:00 UTC 2023` Edited by `admin` on `Sat Dec 16 10:57:00 UTC 2023`
Record UNII	9SK6K682UL
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

DOET

Common Name

English

J71.136E

Code

English

4-ETHYL-2,5-DIMETHOXYAMPHETAMINE

Systematic Name

English

HECATE

Common Name

English

(±)-1-(2,5-DIMETHOXY-4-ETHYLPHENYL)-2-AMINOPROPANE

Systematic Name

English

BENZENEETHANAMINE, 4-ETHYL-2,5-DIMETHOXY-.ALPHA.-METHYL-

Systematic Name

English

(±)-4-ETHYL-2,5-DIMETHOXY-.ALPHA.-METHYLPHENETHYLAMINE

Systematic Name

English

PHENETHYLAMINE, 4-ETHYL-2,5-DIMETHOXY-.ALPHA.-METHYL-

Systematic Name

English

2,5-DIMETHOXY-4-ETHYLAMPHETAMINE

Systematic Name

English

DOE

Common Name

English

Classification Tree Code System Code

WIKIPEDIA

PiHKAL

Created by admin on Sat Dec 16 10:57:00 UTC 2023 , Edited by admin on Sat Dec 16 10:57:00 UTC 2023

WIKIPEDIA

Designer-drugs-2,5-Dimethoxy-4-ethylamphetamine

Created by admin on Sat Dec 16 10:57:00 UTC 2023 , Edited by admin on Sat Dec 16 10:57:00 UTC 2023

DEA NO.

7399

Created by admin on Sat Dec 16 10:57:00 UTC 2023 , Edited by admin on Sat Dec 16 10:57:00 UTC 2023

Code System Code Type Description

INCB IDS CODE

PD 008

Created by admin on Sat Dec 16 10:57:00 UTC 2023 , Edited by admin on Sat Dec 16 10:57:00 UTC 2023

PRIMARY

CAS

22004-32-6

Created by admin on Sat Dec 16 10:57:00 UTC 2023 , Edited by admin on Sat Dec 16 10:57:00 UTC 2023

PRIMARY

EPA CompTox

DTXSID00860585

Created by admin on Sat Dec 16 10:57:00 UTC 2023 , Edited by admin on Sat Dec 16 10:57:00 UTC 2023

PRIMARY

PUBCHEM

27402

Created by admin on Sat Dec 16 10:57:00 UTC 2023 , Edited by admin on Sat Dec 16 10:57:00 UTC 2023

PRIMARY

WIKIPEDIA

2,5-Dimethoxy-4-ethylamphetamine

Created by admin on Sat Dec 16 10:57:00 UTC 2023 , Edited by admin on Sat Dec 16 10:57:00 UTC 2023

PRIMARY

CAYMAN

11141

Created by admin on Sat Dec 16 10:57:00 UTC 2023 , Edited by admin on Sat Dec 16 10:57:00 UTC 2023

PRIMARY

DRUG BANK

DB01467

Created by admin on Sat Dec 16 10:57:00 UTC 2023 , Edited by admin on Sat Dec 16 10:57:00 UTC 2023

PRIMARY

FDA UNII

9SK6K682UL

Created by admin on Sat Dec 16 10:57:00 UTC 2023 , Edited by admin on Sat Dec 16 10:57:00 UTC 2023

PRIMARY

CAS

41538-40-3

Created by admin on Sat Dec 16 10:57:00 UTC 2023 , Edited by admin on Sat Dec 16 10:57:00 UTC 2023

SUPERSEDED

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