Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H8BNO2 |
| Molecular Weight | 172.976 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OB(O)C1=C2N=CC=CC2=CC=C1
InChI
InChIKey=KXJJSKYICDAICD-UHFFFAOYSA-N
InChI=1S/C9H8BNO2/c12-10(13)8-5-1-3-7-4-2-6-11-9(7)8/h1-6,12-13H
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Reactivity of the bifunctional ambiphilic molecule 8-(dimesitylboryl)quinoline: hydrolysis and coordination to Cu(I), Ag(I) and Pd(II). | 2010-12-07 |
|
| Determination of trace alkaline phosphatase by affinity adsorption solid substrate room temperature phosphorimetry based on wheat germ agglutinin labeled with 8-quinolineboronic acid phosphorescent molecular switch and prediction of diseases. | 2010-09-01 |
|
| 8-Quinolineboronic acid as a potential phosphorescent molecular switch for the determination of alpha-fetoprotein variant for the prediction of primary hepatocellular carcinoma. | 2010-03-24 |
|
| Synthesis of aminoboronic acids and their applications in bifunctional catalysis. | 2009-06-16 |
|
| A novel type of fluorescent boronic acid that shows large fluorescence intensity changes upon binding with a carbohydrate in aqueous solution at physiological pH. | 2003-03-24 |
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID00370270
Created by
admin on Mon Mar 31 22:29:21 GMT 2025 , Edited by admin on Mon Mar 31 22:29:21 GMT 2025
|
PRIMARY | |||
|
86-58-8
Created by
admin on Mon Mar 31 22:29:21 GMT 2025 , Edited by admin on Mon Mar 31 22:29:21 GMT 2025
|
PRIMARY | |||
|
m9456
Created by
admin on Mon Mar 31 22:29:21 GMT 2025 , Edited by admin on Mon Mar 31 22:29:21 GMT 2025
|
PRIMARY | Merck Index | ||
|
2734380
Created by
admin on Mon Mar 31 22:29:21 GMT 2025 , Edited by admin on Mon Mar 31 22:29:21 GMT 2025
|
PRIMARY | |||
|
5QS1A25IJ6
Created by
admin on Mon Mar 31 22:29:21 GMT 2025 , Edited by admin on Mon Mar 31 22:29:21 GMT 2025
|
PRIMARY |
SUBSTANCE RECORD