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Details

Stereochemistry ACHIRAL
Molecular Formula C30H26O6
Molecular Weight 482.5238
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4,4'-DIHYDROXY-7,7'-DIMETHYL-5,5'-BIS(1-METHYLETHYL)(8,8'-BI-3H-NAPHTHO(1,8-BC)FURAN)-3,3'-DIONE

SMILES

CC(C)C1=C(O)C(=O)C2=COC3=C2C1=CC(C)=C3C4=C(C)C=C5C6=C4OC=C6C(=O)C(O)=C5C(C)C

InChI

InChIKey=BWOGXQYVDYBLNK-UHFFFAOYSA-N
InChI=1S/C30H26O6/c1-11(2)19-15-7-13(5)21(29-23(15)17(9-35-29)25(31)27(19)33)22-14(6)8-16-20(12(3)4)28(34)26(32)18-10-36-30(22)24(16)18/h7-12,33-34H,1-6H3

HIDE SMILES / InChI

Molecular Formula C30H26O6
Molecular Weight 482.5238
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 Mon Mar 31 22:10:11 GMT 2025
Edited
by admin
on Mon Mar 31 22:10:11 GMT 2025
Record UNII
C8WNV9498S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4,4'-DIHYDROXY-7,7'-DIMETHYL-5,5'-BIS(1-METHYLETHYL)(8,8'-BI-3H-NAPHTHO(1,8-BC)FURAN)-3,3'-DIONE
Systematic Name English
NSC-89310
Preferred Name English
4,4'-DIHYDROXY-5,5'-DIISOPROPYL-7,7'-DIMETHYLBIS(3H-NAPHTHO(1,8-
Common Name English
(8,8'-BI-3H-NAPHTHO(1,8-BC)FURAN)-3,3'-DIONE, 4,4'-DIHYDROXY-7,7'-DIMETHYL-5,5'-BIS(1-METHYLETHYL)-
Systematic Name English
DIANHYDROGOSSYPOL
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID30224050
Created by admin on Mon Mar 31 22:10:11 GMT 2025 , Edited by admin on Mon Mar 31 22:10:11 GMT 2025
PRIMARY
FDA UNII
C8WNV9498S
Created by admin on Mon Mar 31 22:10:11 GMT 2025 , Edited by admin on Mon Mar 31 22:10:11 GMT 2025
PRIMARY
NSC
89310
Created by admin on Mon Mar 31 22:10:11 GMT 2025 , Edited by admin on Mon Mar 31 22:10:11 GMT 2025
PRIMARY
CAS
73728-76-4
Created by admin on Mon Mar 31 22:10:11 GMT 2025 , Edited by admin on Mon Mar 31 22:10:11 GMT 2025
PRIMARY
PUBCHEM
5380201
Created by admin on Mon Mar 31 22:10:11 GMT 2025 , Edited by admin on Mon Mar 31 22:10:11 GMT 2025
PRIMARY