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Details

Stereochemistry RACEMIC
Molecular Formula C30H42BrNO
Molecular Weight 512.565
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 6-BROMO-.ALPHA.-(DIHEPTYLAMINOMETHYL)-9-PHENANTHRENEMETHANOL, (±)-

SMILES

CCCCCCCN(CCCCCCC)CC(O)C1=CC2=CC=CC=C2C3=C1C=CC(Br)=C3

InChI

InChIKey=BWNCHMAKZSGSMP-UHFFFAOYSA-N
InChI=1S/C30H42BrNO/c1-3-5-7-9-13-19-32(20-14-10-8-6-4-2)23-30(33)29-21-24-15-11-12-16-26(24)28-22-25(31)17-18-27(28)29/h11-12,15-18,21-22,30,33H,3-10,13-14,19-20,23H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C30H42BrNO
Molecular Weight 512.565
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 Mon Mar 31 22:44:04 GMT 2025
Edited
by admin
on Mon Mar 31 22:44:04 GMT 2025
Record UNII
1IP26U1AXI
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
6-BROMO-.ALPHA.-(DIHEPTYLAMINOMETHYL)-9-PHENANTHRENEMETHANOL, (±)-
Systematic Name English
NIH-1577
Preferred Name English
SN-13465
Code English
WR-33063
Code English
6-BROMO-.ALPHA.-(DIHEPTYLAMINOMETHYL)PHENANTHRENEMETHANOL
Systematic Name English
9-PHENANTHRENEMETHANOL, 6-BROMO-.ALPHA.-((DIHEPTYLAMINO)METHYL)-
Systematic Name English
(±)-6-BROMO-ALPHA-((DIHEPTYLAMINO)METHYL)-9-PHENANTHRENEMETHANOL
Systematic Name English
DL-.ALPHA.-DIHEPTYLAMINOMETHYL-6-BROMO-9-PHENANTHRENEMETHANOL
Systematic Name English
N,N-DIHEPTYL-2-HYDROXY-2-(3-BROMO-10-PHENANTHRYL)ETHYLAMINE
Systematic Name English
Code System Code Type Description
PUBCHEM
31783
Created by admin on Mon Mar 31 22:44:04 GMT 2025 , Edited by admin on Mon Mar 31 22:44:04 GMT 2025
PRIMARY
CAS
56924-18-6
Created by admin on Mon Mar 31 22:44:04 GMT 2025 , Edited by admin on Mon Mar 31 22:44:04 GMT 2025
SUPERSEDED
EPA CompTox
DTXSID00865333
Created by admin on Mon Mar 31 22:44:04 GMT 2025 , Edited by admin on Mon Mar 31 22:44:04 GMT 2025
PRIMARY
FDA UNII
1IP26U1AXI
Created by admin on Mon Mar 31 22:44:04 GMT 2025 , Edited by admin on Mon Mar 31 22:44:04 GMT 2025
PRIMARY
CAS
27022-39-5
Created by admin on Mon Mar 31 22:44:04 GMT 2025 , Edited by admin on Mon Mar 31 22:44:04 GMT 2025
PRIMARY