Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H8O2 |
Molecular Weight | 160.1693 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC2=CC=C(O)C=C2C=C1
InChI
InChIKey=MNZMMCVIXORAQL-UHFFFAOYSA-N
InChI=1S/C10H8O2/c11-9-3-1-7-5-10(12)4-2-8(7)6-9/h1-6,11-12H
Molecular Formula | C10H8O2 |
Molecular Weight | 160.1693 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Hydroxynaphthaldehyde phosphate derivatives as potent covalent Schiff base inhibitors of fructose-1,6-bisphosphate aldolase. | 2005 Apr 12 |
|
Regiospecific oxidation of naphthalene and fluorene by toluene monooxygenases and engineered toluene 4-monooxygenases of Pseudomonas mendocina KR1. | 2005 Apr 5 |
|
The influence of aromatic residues in hydraphile spacer units: assay by ion selective electrode methods and in bacteria. | 2005 May 2 |
|
Toward high-generation rotaxane dendrimers that incorporate a ring component on every branch: noncovalent synthesis of a dendritic [10]pseudorotaxane with 13 molecular components. | 2007 Jun 4 |
|
4,4'-(2,6-Dihydroxy-naphthalene-1,5-diyldimethyl-ene)dipyridinium bis-(per-chlorate). | 2008 May 30 |
|
Chromane derivatives of small aromatic molecules: Chemoenzymatic synthesis and growth inhibitory activity on human tumor cell line LoVo WT. | 2009 Aug 15 |
|
Experimental and theoretical studies on constitutional isomers of 2,6-dihydroxynaphthalene carbaldehydes. Effects of resonance-assisted hydrogen bonding on the electronic absorption spectra. | 2009 Jan 16 |
|
New thermal and microbial resistant metal-containing epoxy polymers. | 2010 |
|
Synthesis, properties, crystal structures, and semiconductor characteristics of naphtho[1,2-b:5,6-b']dithiophene and -diselenophene derivatives. | 2010 Feb 19 |
|
A light-controlled molecular brake with complete ON-OFF rotation. | 2010 Mar 15 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:05:05 GMT 2023
by
admin
on
Fri Dec 15 19:05:05 GMT 2023
|
Record UNII |
4XX2ND0257
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Code | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
C483528
Created by
admin on Fri Dec 15 19:05:05 GMT 2023 , Edited by admin on Fri Dec 15 19:05:05 GMT 2023
|
PRIMARY | |||
|
209-465-6
Created by
admin on Fri Dec 15 19:05:05 GMT 2023 , Edited by admin on Fri Dec 15 19:05:05 GMT 2023
|
PRIMARY | |||
|
581-43-1
Created by
admin on Fri Dec 15 19:05:05 GMT 2023 , Edited by admin on Fri Dec 15 19:05:05 GMT 2023
|
PRIMARY | |||
|
DTXSID7060384
Created by
admin on Fri Dec 15 19:05:05 GMT 2023 , Edited by admin on Fri Dec 15 19:05:05 GMT 2023
|
PRIMARY | |||
|
4XX2ND0257
Created by
admin on Fri Dec 15 19:05:05 GMT 2023 , Edited by admin on Fri Dec 15 19:05:05 GMT 2023
|
PRIMARY | |||
|
62687
Created by
admin on Fri Dec 15 19:05:05 GMT 2023 , Edited by admin on Fri Dec 15 19:05:05 GMT 2023
|
PRIMARY | |||
|
93552
Created by
admin on Fri Dec 15 19:05:05 GMT 2023 , Edited by admin on Fri Dec 15 19:05:05 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
PARENT -> METABOLITE |
IN VITRO
|