Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H17NO2 |
| Molecular Weight | 231.2903 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCN(CC)C1=CC2=C(C=C1)C(C)=CC(=O)O2
InChI
InChIKey=AFYCEAFSNDLKSX-UHFFFAOYSA-N
InChI=1S/C14H17NO2/c1-4-15(5-2)11-6-7-12-10(3)8-14(16)17-13(12)9-11/h6-9H,4-5H2,1-3H3
| Molecular Formula | C14H17NO2 |
| Molecular Weight | 231.2903 |
| 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 |
|---|---|---|
| Effect of fluorescent whitening agent on the transcription of cell damage-related genes in zebrafish embryos. | 2012-09 |
|
| Polymeric micelles in anticancer therapy: targeting, imaging and triggered release. | 2010-12 |
|
| Identification of chemical compounds that induce HIF-1alpha activity. | 2009-11 |
|
| Fluorescence-based sensing of p-nitrophenol and p-nitrophenyl substituent organophosphates. | 2007-07-16 |
|
| Effect of donor-acceptor interaction strength on excitation energy migration and diffusion at high donor concentrations. | 2006-10-14 |
|
| Prediction of genotoxicity of chemical compounds by statistical learning methods. | 2005-06 |
|
| A protecting group for carboxylic acids that can be photolyzed by visible light. | 2005-05-17 |
|
| [7-(Dialkylamino)coumarin-4-yl]methyl-Caged Compounds as Ultrafast and Effective Long-Wavelength Phototriggers of 8-Bromo-Substituted Cyclic Nucleotides. | 2003-05-09 |
|
| Rotational diffusion of the 7-diethylamino-4-methylcoumarin C1 dye molecule in polar protic and aprotic solvents. | 2003-03 |
|
| Spatial relationship between the prodan site, Trp-214, and Cys-34 residues in human serum albumin and loss of structure through incremental unfolding. | 2002-06-11 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:54:55 GMT 2025
by
admin
on
Mon Mar 31 20:54:55 GMT 2025
|
| Record UNII |
1SFJ7F6R2C
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Official Name | English | ||
|
Systematic Name | English | ||
|
Brand Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Brand Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
202-068-9
Created by
admin on Mon Mar 31 20:54:55 GMT 2025 , Edited by admin on Mon Mar 31 20:54:55 GMT 2025
|
PRIMARY | |||
|
7050
Created by
admin on Mon Mar 31 20:54:55 GMT 2025 , Edited by admin on Mon Mar 31 20:54:55 GMT 2025
|
PRIMARY | |||
|
61830
Created by
admin on Mon Mar 31 20:54:55 GMT 2025 , Edited by admin on Mon Mar 31 20:54:55 GMT 2025
|
PRIMARY | |||
|
1SFJ7F6R2C
Created by
admin on Mon Mar 31 20:54:55 GMT 2025 , Edited by admin on Mon Mar 31 20:54:55 GMT 2025
|
PRIMARY | |||
|
1737792
Created by
admin on Mon Mar 31 20:54:55 GMT 2025 , Edited by admin on Mon Mar 31 20:54:55 GMT 2025
|
PRIMARY | |||
|
4244
Created by
admin on Mon Mar 31 20:54:55 GMT 2025 , Edited by admin on Mon Mar 31 20:54:55 GMT 2025
|
PRIMARY | |||
|
DTXSID9025035
Created by
admin on Mon Mar 31 20:54:55 GMT 2025 , Edited by admin on Mon Mar 31 20:54:55 GMT 2025
|
PRIMARY | |||
|
91-44-1
Created by
admin on Mon Mar 31 20:54:55 GMT 2025 , Edited by admin on Mon Mar 31 20:54:55 GMT 2025
|
PRIMARY | |||
|
51938
Created by
admin on Mon Mar 31 20:54:55 GMT 2025 , Edited by admin on Mon Mar 31 20:54:55 GMT 2025
|
PRIMARY |