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Details

Stereochemistry RACEMIC
Molecular Formula C19H38O
Molecular Weight 282.5044
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DISPARLURE

SMILES

CCCCCCCCCC[C@H]1O[C@H]1CCCCC(C)C

InChI

InChIKey=HFOFYNMWYRXIBP-MOPGFXCFSA-N
InChI=1S/C19H38O/c1-4-5-6-7-8-9-10-11-15-18-19(20-18)16-13-12-14-17(2)3/h17-19H,4-16H2,1-3H3/t18-,19+/m1/s1

HIDE SMILES / InChI

Molecular Formula C19H38O
Molecular Weight 282.5044
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 Fri Dec 15 18:59:29 GMT 2023
Edited
by admin
on Fri Dec 15 18:59:29 GMT 2023
Record UNII
1FU18G2315
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DISPARLURE
Common Name English
(2R,3S)-REL-2-DECYL-3-(5-METHYLHEXYL)OXIRANE
Common Name English
DISPARLURE (±)-CIS-FORM [MI]
Common Name English
DISPARLURE, CIS-(±)-
Common Name English
7,8-EPOXY-2-METHYLOCTADECANE, CIS-
Common Name English
DISRUPT II GM
Brand Name English
ENT-34886
Code English
OXIRANE, 2-DECYL-3-(5-METHYLHEXYL)-, (2R,3S)-REL-
Systematic Name English
(7RS,8SR)-7,8-EPOXY-2-METHYLOCTADECANE
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 114301
Created by admin on Fri Dec 15 18:59:29 GMT 2023 , Edited by admin on Fri Dec 15 18:59:29 GMT 2023
Code System Code Type Description
MERCK INDEX
m4673
Created by admin on Fri Dec 15 18:59:29 GMT 2023 , Edited by admin on Fri Dec 15 18:59:29 GMT 2023
PRIMARY Merck Index
MESH
C001150
Created by admin on Fri Dec 15 18:59:29 GMT 2023 , Edited by admin on Fri Dec 15 18:59:29 GMT 2023
PRIMARY
ECHA (EC/EINECS)
249-861-6
Created by admin on Fri Dec 15 18:59:29 GMT 2023 , Edited by admin on Fri Dec 15 18:59:29 GMT 2023
PRIMARY
PUBCHEM
62850
Created by admin on Fri Dec 15 18:59:29 GMT 2023 , Edited by admin on Fri Dec 15 18:59:29 GMT 2023
PRIMARY
ALANWOOD
disparlure
Created by admin on Fri Dec 15 18:59:29 GMT 2023 , Edited by admin on Fri Dec 15 18:59:29 GMT 2023
PRIMARY
CAS
29804-22-6
Created by admin on Fri Dec 15 18:59:29 GMT 2023 , Edited by admin on Fri Dec 15 18:59:29 GMT 2023
PRIMARY
FDA UNII
1FU18G2315
Created by admin on Fri Dec 15 18:59:29 GMT 2023 , Edited by admin on Fri Dec 15 18:59:29 GMT 2023
PRIMARY
EPA CompTox
DTXSID4035548
Created by admin on Fri Dec 15 18:59:29 GMT 2023 , Edited by admin on Fri Dec 15 18:59:29 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE