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Details

Stereochemistry MIXED
Molecular Formula C15H26O2
Molecular Weight 238.3657
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NEROLIDOL OXIDE I

SMILES

[H][C@@]1(CC[C@](C)(O1)C=C)C(C)(O)CCC=C(C)C

InChI

InChIKey=OIVTVPOJCWXSIC-GRKKQISMSA-N
InChI=1S/C15H26O2/c1-6-14(4)11-9-13(17-14)15(5,16)10-7-8-12(2)3/h6,8,13,16H,1,7,9-11H2,2-5H3/t13-,14-,15?/m1/s1

HIDE SMILES / InChI

Molecular Formula C15H26O2
Molecular Weight 238.3657
Charge 0
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 2 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 01:40:01 GMT 2023
Edited
by admin
on Sat Dec 16 01:40:01 GMT 2023
Record UNII
8CDV2ZNM24
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NEROLIDOL OXIDE I
Common Name English
2-FURANMETHANOL, 5-ETHENYLTETRAHYDRO-.ALPHA.,5-DIMETHYL-.ALPHA.-(4-METHYL-3-PENTENYL)-, (2.ALPHA.,5.ALPHA.)-(PARTIAL)-
Common Name English
FEMA NO. 4549
Code English
2-FURANMETHANOL, 5-ETHENYLTETRAHYDRO-.ALPHA.,5-DIMETHYL-.ALPHA.-(4-METHYL-3-PENTENYL)-, (2R,5S)-REL-
Common Name English
NEROLIDOL OXIDE
Systematic Name English
2-FURANMETHANOL, 5-ETHENYLTETRAHYDRO-.ALPHA.,5-DIMETHYL-.ALPHA.-(4-METHYL-3-PENTEN-1-YL)-, (2R,5S)-REL-
Common Name English
Classification Tree Code System Code
JECFA EVALUATION NEROLIDOL OXIDE
Created by admin on Sat Dec 16 01:40:01 GMT 2023 , Edited by admin on Sat Dec 16 01:40:01 GMT 2023
Code System Code Type Description
FDA UNII
8CDV2ZNM24
Created by admin on Sat Dec 16 01:40:01 GMT 2023 , Edited by admin on Sat Dec 16 01:40:01 GMT 2023
PRIMARY
EPA CompTox
DTXSID80171762
Created by admin on Sat Dec 16 01:40:01 GMT 2023 , Edited by admin on Sat Dec 16 01:40:01 GMT 2023
PRIMARY
PUBCHEM
71587598
Created by admin on Sat Dec 16 01:40:01 GMT 2023 , Edited by admin on Sat Dec 16 01:40:01 GMT 2023
PRIMARY
JECFA MONOGRAPH
1986
Created by admin on Sat Dec 16 01:40:01 GMT 2023 , Edited by admin on Sat Dec 16 01:40:01 GMT 2023
PRIMARY
CAS
185253-84-3
Created by admin on Sat Dec 16 01:40:01 GMT 2023 , Edited by admin on Sat Dec 16 01:40:01 GMT 2023
PRIMARY