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Details

Stereochemistry ACHIRAL
Molecular Formula C13H18O
Molecular Weight 190.2814
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HEPTANOPHENONE

SMILES

CCCCCCC(=O)C1=CC=CC=C1

InChI

InChIKey=UXMQORVHJMUQFD-UHFFFAOYSA-N
InChI=1S/C13H18O/c1-2-3-4-8-11-13(14)12-9-6-5-7-10-12/h5-7,9-10H,2-4,8,11H2,1H3

HIDE SMILES / InChI

Molecular Formula C13H18O
Molecular Weight 190.2814
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Effect of surfactant counterion and organic modifier on the properties of surfactant vesicles in electrokinetic chromatography.
2005 Aug
Inhibition of carbonyl reductase activity in pig heart by alkyl phenyl ketones.
2007 Feb
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:46:42 GMT 2023
Edited
by admin
on Fri Dec 15 19:46:42 GMT 2023
Record UNII
KX07WP06JY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HEPTANOPHENONE
Systematic Name English
1-HEPTANONE, 1-PHENYL-
Systematic Name English
1-PHENYLHEPTANONE
Systematic Name English
HEXYL PHENYL KETONE
Systematic Name English
N-HEXYL PHENYL KETONE
Common Name English
1-PHENYL-1-HEPTANONE
Systematic Name English
ENANTHOPHENONE
Systematic Name English
1-OXO-1-PHENYLHEPTANE
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID9048194
Created by admin on Fri Dec 15 19:46:42 GMT 2023 , Edited by admin on Fri Dec 15 19:46:42 GMT 2023
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FDA UNII
KX07WP06JY
Created by admin on Fri Dec 15 19:46:42 GMT 2023 , Edited by admin on Fri Dec 15 19:46:42 GMT 2023
PRIMARY
CAS
1671-75-6
Created by admin on Fri Dec 15 19:46:42 GMT 2023 , Edited by admin on Fri Dec 15 19:46:42 GMT 2023
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PUBCHEM
74282
Created by admin on Fri Dec 15 19:46:42 GMT 2023 , Edited by admin on Fri Dec 15 19:46:42 GMT 2023
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ECHA (EC/EINECS)
216-802-0
Created by admin on Fri Dec 15 19:46:42 GMT 2023 , Edited by admin on Fri Dec 15 19:46:42 GMT 2023
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