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Details

Stereochemistry ACHIRAL
Molecular Formula C13H16
Molecular Weight 172.2661
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,2-DIHYDRO-1,1,6-TRIMETHYLNAPHTHALENE

SMILES

CC1=CC=C2C(C=CCC2(C)C)=C1

InChI

InChIKey=RTUMCNDCAVLXEP-UHFFFAOYSA-N
InChI=1S/C13H16/c1-10-6-7-12-11(9-10)5-4-8-13(12,2)3/h4-7,9H,8H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C13H16
Molecular Weight 172.2661
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Timing of cluster light environment manipulation during grape development affects C13 norisoprenoid and carotenoid concentrations in Riesling.
2010-06-09
Free and hydrolytically released volatile compounds of Vitis vinifera L. cv. Fiano grapes as odour-active constituents of Fiano wine.
2008-07-21
Influence of plant water status on the production of C13-norisoprenoid precursors in Vitis vinifera L. Cv. cabernet sauvignon grape berries.
2007-05-30
Quantitative analysis, occurrence, and stability of (E)-1-(2,3,6-Trimethylphenyl)buta-1,3-diene in wine.
2005-05-04
Identification of key odorants related to the typical aroma of oxidation-spoiled white wines.
2003-02-26
3,4-Dihydroxy-7,8-dihydro-beta-ionone 3-O-beta-D-glucopyranoside and other glycosidic constituents from apple leaves.
2002-04
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:13:47 GMT 2025
Edited
by admin
on Mon Mar 31 19:13:47 GMT 2025
Record UNII
01HD1KNX99
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DEHYDRO-AR-IONENE
Preferred Name English
1,2-DIHYDRO-1,1,6-TRIMETHYLNAPHTHALENE
Systematic Name English
1,1,6-TRIMETHYL-1,2-DIHYDRONAPHTHALENE
Systematic Name English
NAPHTHALENE, 1,2-DIHYDRO-1,1,6-TRIMETHYL-
Systematic Name English
Code System Code Type Description
PUBCHEM
121677
Created by admin on Mon Mar 31 19:13:47 GMT 2025 , Edited by admin on Mon Mar 31 19:13:47 GMT 2025
PRIMARY
MESH
C573721
Created by admin on Mon Mar 31 19:13:47 GMT 2025 , Edited by admin on Mon Mar 31 19:13:47 GMT 2025
PRIMARY
CAS
30364-38-6
Created by admin on Mon Mar 31 19:13:47 GMT 2025 , Edited by admin on Mon Mar 31 19:13:47 GMT 2025
PRIMARY
EPA CompTox
DTXSID30184443
Created by admin on Mon Mar 31 19:13:47 GMT 2025 , Edited by admin on Mon Mar 31 19:13:47 GMT 2025
PRIMARY
ECHA (EC/EINECS)
250-150-8
Created by admin on Mon Mar 31 19:13:47 GMT 2025 , Edited by admin on Mon Mar 31 19:13:47 GMT 2025
PRIMARY
FDA UNII
01HD1KNX99
Created by admin on Mon Mar 31 19:13:47 GMT 2025 , Edited by admin on Mon Mar 31 19:13:47 GMT 2025
PRIMARY