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Details

Stereochemistry ABSOLUTE
Molecular Formula C15H20O
Molecular Weight 216.3187
Optical Activity ( + )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Mutisianthol

SMILES

C[C@@H]1C[C@@H](C=C(C)C)C2=CC(C)=C(O)C=C12

InChI

InChIKey=SVNPNOPENVFTBB-ZYHUDNBSSA-N
InChI=1S/C15H20O/c1-9(2)5-12-6-10(3)13-8-15(16)11(4)7-14(12)13/h5,7-8,10,12,16H,6H2,1-4H3/t10-,12-/m1/s1

HIDE SMILES / InChI

Molecular Formula C15H20O
Molecular Weight 216.3187
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Wed Apr 02 09:06:24 GMT 2025
Edited
by admin
on Wed Apr 02 09:06:24 GMT 2025
Record UNII
F69DJ259PV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Mutisianthol
Common Name English
(+)-MUTISIANTHOL
Preferred Name English
1H-INDEN-5-OL, 2,3-DIHYDRO-3,6-DIMETHYL-1-(2-METHYL-1-PROPENYL)-, (1S,3R)-
Systematic Name English
MUTISIANTHOL, (+)-
Common Name English
1H-INDEN-5-OL, 2,3-DIHYDRO-3,6-DIMETHYL-1-(2-METHYL-1-PROPEN-1-YL)-, (1S,3R)-
Systematic Name English
(1S,3R)-2,3-DIHYDRO-3,6-DIMETHYL-1-(2-METHYL-1-PROPEN-1-YL)-1H-INDEN-5-OL
Systematic Name English
1H-INDEN-5-OL, 2,3-DIHYDRO-3,6-DIMETHYL-1-(2-METHYL-1-PROPENYL)-, TRANS-(+)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID20479072
Created by admin on Wed Apr 02 09:06:24 GMT 2025 , Edited by admin on Wed Apr 02 09:06:24 GMT 2025
PRIMARY
CAS
70855-59-3
Created by admin on Wed Apr 02 09:06:24 GMT 2025 , Edited by admin on Wed Apr 02 09:06:24 GMT 2025
PRIMARY
FDA UNII
F69DJ259PV
Created by admin on Wed Apr 02 09:06:24 GMT 2025 , Edited by admin on Wed Apr 02 09:06:24 GMT 2025
PRIMARY
PUBCHEM
12168490
Created by admin on Wed Apr 02 09:06:24 GMT 2025 , Edited by admin on Wed Apr 02 09:06:24 GMT 2025
PRIMARY
WIKIPEDIA
Mutisianthol
Created by admin on Wed Apr 02 09:06:24 GMT 2025 , Edited by admin on Wed Apr 02 09:06:24 GMT 2025
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER