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Details

Stereochemistry ACHIRAL
Molecular Formula C10H8O
Molecular Weight 144.1699
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-NAPHTHOL

SMILES

OC1=C2C=CC=CC2=CC=C1

InChI

InChIKey=KJCVRFUGPWSIIH-UHFFFAOYSA-N
InChI=1S/C10H8O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7,11H

HIDE SMILES / InChI
Molecular Formula C10H8O
Molecular Weight 144.1699
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

2016
484
PubMed

PubMed

TitleDatePubMed
Sorption of 1-naphthol to soil and geologic samples with varying diagenetic properties.
2001 Aug
A structural account of substrate and inhibitor specificity differences between two naphthol reductases.
2001 Jul 31
Reaction kinetics for laccase-catalyzed polymerization of 1-naphthol.
2001 Oct
Concentration-dependent effects of the esterase inhibitor BNPP on macrophage migration and myelin phagocytosis.
2001 Oct 19
Resistance of aphis gossypii (Homoptera: Aphididae) to fenvalerate and imidacloprid and activities of detoxification enzymes on cotton and cucumber.
2002 Apr
4-Aryloxybutenolides as "chiral aldehyde" equivalents: an efficient enantioselective synthesis of (+)-brefeldin a.
2002 Aug 14
Thin-layer chromatography and electrospray mass spectrometry coupled using a surface sampling probe.
2002 Dec 15
First total synthesis of the 7,3'-linked naphthylisoquinoline alkaloid ancistrocladidine.
2002 Feb 21
A chiral molecular square with metallo-corners for enantioselective sensing.
2002 May 1
Synthesis of novel BINOL-derived chiral bisphosphorus ligands and their application in catalytic asymmetric hydrogenation.
2002 May 21
Gold bands as a suitable surface for enzyme immunoassays.
2002 Sep
Solid-phase microextraction from small volumes of sample in a glass capillary.
2003 Feb 21
Catalytic activities of cytochrome P450 enzymes and UDP-glucuronosyltransferases involved in drug metabolism in rat everted sacs and intestinal microsomes.
2003 Jan
Amperometric biosensors based on recombinant laccases for phenols determination.
2003 Mar
Patents

Patents

JP2000038430A
1
JP2000219686A
1
JP2000303006A
1
JP2001011160A
1
JP2001106667A
1
JP2001171234A
1
JP2001226454A
1
JP2001302764A
1
JP2002138096A
1
JP2002302465A
1
JP2002534542A
2
JP2002544121A
1
JP2003012773A
1
JP2003201324A
1
JP2003507133A
1
JP2004224762A
3
JP2004269607A
1
JP2004534787A
1
JP2005097601A
1
JP2005220049A
1
JP2006002039A
1
JP2006506416A
1
JP2007277102A
1
JP2007302603A
1
JP2008001851A
1
JP2008001852A
1
JP2008506826A
1
JP2009300978A
1
JP2009503121A
1
JP2011511317A
1
JP4659743B2
1
JPH01186856A
1
JPH01190649A
1
JPH01305058A
1
JPH0240352A
1
JPH0321627A
1
JPH03239738A
1
JPH04155939A
1
JPH04155940A
1
JPH04198314A
1
JPH04226131A
1
JPH04332714A
1
JPH05132542A
1
JPH05230389A
3
JPH05279585A
1
JPH05299537A
1
JPH0570554A
1
JPH0586170A
1
JPH0593037A
1
JPH0593040A
1
JPH06107771A
1
Substance Class Chemical
Created
by admin
on Thu Jul 06 10:23:53 UTC 2023
Edited
by admin
on Thu Jul 06 10:23:53 UTC 2023
Record UNII
2A71EAQ389
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1-NAPHTHOL
HSDB   INCI   MI  
INCI  
Official Name English
DULOXETINE IMPURITY D [USP IMPURITY]
Common Name English
.ALPHA.-NAPHTHOL
Systematic Name English
1-NAPHTHALENOL
Systematic Name English
1-NAPHTHOL [INCI]
Common Name English
ALPHA-NAPHTHOL
Systematic Name English
NSC-9586
Code English
1-HYDROXYNAPHTHALENE
Systematic Name English
NAPHTHALEN-1-OL
Systematic Name English
1-NAPHTOL-
Common Name English
DULOXETINE IMPURITY D
USP  
Common Name English
1-NAPHTHOL [MI]
Common Name English
NAPHTHOL, 1-
Systematic Name English
1-NAPHTHOL [HSDB]
Common Name English
DULOXETINE HYDROCHLORIDE IMPURITY D [EP IMPURITY]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 206500
Created by admin on Thu Jul 06 10:23:53 UTC 2023 , Edited by admin on Thu Jul 06 10:23:53 UTC 2023
Code System Code Type Description
CHEBI
10319
Created by admin on Thu Jul 06 10:23:53 UTC 2023 , Edited by admin on Thu Jul 06 10:23:53 UTC 2023
PRIMARY
DAILYMED
2A71EAQ389
Created by admin on Thu Jul 06 10:23:53 UTC 2023 , Edited by admin on Thu Jul 06 10:23:53 UTC 2023
PRIMARY
RS_ITEM_NUM
1A01070
Created by admin on Thu Jul 06 10:23:53 UTC 2023 , Edited by admin on Thu Jul 06 10:23:53 UTC 2023
PRIMARY
WIKIPEDIA
1-Naphthol
Created by admin on Thu Jul 06 10:23:53 UTC 2023 , Edited by admin on Thu Jul 06 10:23:53 UTC 2023
PRIMARY
FDA UNII
2A71EAQ389
Created by admin on Thu Jul 06 10:23:53 UTC 2023 , Edited by admin on Thu Jul 06 10:23:53 UTC 2023
PRIMARY
MESH
C029350
Created by admin on Thu Jul 06 10:23:53 UTC 2023 , Edited by admin on Thu Jul 06 10:23:53 UTC 2023
PRIMARY
HSDB
2650
Created by admin on Thu Jul 06 10:23:53 UTC 2023 , Edited by admin on Thu Jul 06 10:23:53 UTC 2023
PRIMARY
PUBCHEM
7005
Created by admin on Thu Jul 06 10:23:53 UTC 2023 , Edited by admin on Thu Jul 06 10:23:53 UTC 2023
PRIMARY
RXCUI
1740233
Created by admin on Thu Jul 06 10:23:53 UTC 2023 , Edited by admin on Thu Jul 06 10:23:53 UTC 2023
PRIMARY
EPA CompTox
DTXSID6021793
Created by admin on Thu Jul 06 10:23:53 UTC 2023 , Edited by admin on Thu Jul 06 10:23:53 UTC 2023
PRIMARY
CAS
90-15-3
Created by admin on Thu Jul 06 10:23:53 UTC 2023 , Edited by admin on Thu Jul 06 10:23:53 UTC 2023
PRIMARY
ALANWOOD
1-naphthol
Created by admin on Thu Jul 06 10:23:53 UTC 2023 , Edited by admin on Thu Jul 06 10:23:53 UTC 2023
PRIMARY
MERCK INDEX
M7738
Created by admin on Thu Jul 06 10:23:53 UTC 2023 , Edited by admin on Thu Jul 06 10:23:53 UTC 2023
PRIMARY Merck Index
NSC
9586
Created by admin on Thu Jul 06 10:23:53 UTC 2023 , Edited by admin on Thu Jul 06 10:23:53 UTC 2023
PRIMARY
ECHA (EC/EINECS)
201-969-4
Created by admin on Thu Jul 06 10:23:53 UTC 2023 , Edited by admin on Thu Jul 06 10:23:53 UTC 2023
PRIMARY
Related Record Type Details
Structure of NAPHTHALENE
PARENT -> METABOLITE
IN VITRO
Structure of 1-NAPHTHYL GLUCURONIDE
METABOLITE -> PARENT
IN-VITRO
NIH
NCATS
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