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Details

Stereochemistry RACEMIC
Molecular Formula C13H12O2
Molecular Weight 200.2332
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLYCIDYL 1-NAPHTHYL ETHER

SMILES

C(OC1=CC=CC2=CC=CC=C12)C3CO3

InChI

InChIKey=QYYCPWLLBSSFBW-UHFFFAOYSA-N
InChI=1S/C13H12O2/c1-2-6-12-10(4-1)5-3-7-13(12)15-9-11-8-14-11/h1-7,11H,8-9H2

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis, biological evaluation and mechanistic studies of totarol amino alcohol derivatives as potential antimalarial agents.
2012-01-15
Patents
Name Type Language
NSC-632
Preferred Name English
GLYCIDYL 1-NAPHTHYL ETHER
Systematic Name English
(±)-1-(1-NAPHTHYLOXY)-2,3-EPOXYPROPANE
Systematic Name English
1-(2,3-EPOXYPROPOXY)NAPHTHALENE
Systematic Name English
GLYCIDYL .ALPHA.-NAPHTHYL ETHER
Systematic Name English
NAPHTHALENE, 1-(2,3-EPOXYPROPOXY)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID501030986
Created by admin on Mon Mar 31 22:42:06 GMT 2025 , Edited by admin on Mon Mar 31 22:42:06 GMT 2025
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NSC
632
Created by admin on Mon Mar 31 22:42:06 GMT 2025 , Edited by admin on Mon Mar 31 22:42:06 GMT 2025
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PUBCHEM
91521
Created by admin on Mon Mar 31 22:42:06 GMT 2025 , Edited by admin on Mon Mar 31 22:42:06 GMT 2025
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FDA UNII
07FN14F351
Created by admin on Mon Mar 31 22:42:06 GMT 2025 , Edited by admin on Mon Mar 31 22:42:06 GMT 2025
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ECHA (EC/EINECS)
219-555-7
Created by admin on Mon Mar 31 22:42:06 GMT 2025 , Edited by admin on Mon Mar 31 22:42:06 GMT 2025
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CAS
2461-42-9
Created by admin on Mon Mar 31 22:42:06 GMT 2025 , Edited by admin on Mon Mar 31 22:42:06 GMT 2025
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