U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C11H16BrNO2
Molecular Weight 274.154
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-BR-3,5-DMA

SMILES

COC1=CC(CC(C)N)=CC(OC)=C1Br

InChI

InChIKey=FAVLJTSHWBEOMA-UHFFFAOYSA-N
InChI=1S/C11H16BrNO2/c1-7(13)4-8-5-9(14-2)11(12)10(6-8)15-3/h5-7H,4,13H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C11H16BrNO2
Molecular Weight 274.154
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 17:11:10 GMT 2023
Edited
by admin
on Sat Dec 16 17:11:10 GMT 2023
Record UNII
5BN3H3UZ8R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-BR-3,5-DMA
Common Name English
PHENETHYLAMINE, 4-BROMO-3,5-DIMETHOXY-.ALPHA.-METHYL-
Systematic Name English
4-BROMO-3,5-DIMETHOXYAMPHETAMINE
Common Name English
BENZENEETHANAMINE, 4-BROMO-3,5-DIMETHOXY-.ALPHA.-METHYL-
Systematic Name English
3,5-DIMETHOXY-4-BROMOAMPHETAMINE
Systematic Name English
4-BROMO-3,5-DIMETHOXY-.ALPHA.-METHYLBENZENEETHANAMINE
Systematic Name English
1-(4-BROMO-3,5-DIMETHOXYPHENYL)PROPAN-2-AMINE
Common Name English
Classification Tree Code System Code
WIKIPEDIA PiHKAL
Created by admin on Sat Dec 16 17:11:10 GMT 2023 , Edited by admin on Sat Dec 16 17:11:10 GMT 2023
Code System Code Type Description
WIKIPEDIA
4-Bromo-3,5-dimethoxyamphetamine
Created by admin on Sat Dec 16 17:11:10 GMT 2023 , Edited by admin on Sat Dec 16 17:11:10 GMT 2023
PRIMARY
EPA CompTox
DTXSID30276857
Created by admin on Sat Dec 16 17:11:10 GMT 2023 , Edited by admin on Sat Dec 16 17:11:10 GMT 2023
PRIMARY
CAS
32156-34-6
Created by admin on Sat Dec 16 17:11:10 GMT 2023 , Edited by admin on Sat Dec 16 17:11:10 GMT 2023
PRIMARY
PUBCHEM
208044
Created by admin on Sat Dec 16 17:11:10 GMT 2023 , Edited by admin on Sat Dec 16 17:11:10 GMT 2023
PRIMARY
FDA UNII
5BN3H3UZ8R
Created by admin on Sat Dec 16 17:11:10 GMT 2023 , Edited by admin on Sat Dec 16 17:11:10 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY