Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H7NO3 |
| Molecular Weight | 165.1461 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)C1=CC=CC(=C1)[N+]([O-])=O
InChI
InChIKey=ARKIFHPFTHVKDT-UHFFFAOYSA-N
InChI=1S/C8H7NO3/c1-6(10)7-3-2-4-8(5-7)9(11)12/h2-5H,1H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis of some phenacyl derivatives of 1-methyl-7-methoxy-beta-carboline and their behavioural study. | 2003 Jan |
|
| (2E)-3-(4-Methyl-phen-yl)-1-(3-nitro-phen-yl)prop-2-en-1-one. | 2007 Dec 6 |
|
| 2-Bromo-1-(3-nitro-phen-yl)ethanone. | 2010 Dec 4 |
|
| New reagents for increasing ESI multiple charging of proteins and protein complexes. | 2010 Jan |
|
| Synthesis, Characterization, and Biological Evaluation of certain 6-methyl-2(3H)-benzo-1, 3-thiazolyl-1'-ethylidene-2-(o, p- Substituted Acetophenones) Hydrazine Analogs. | 2010 Oct |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
2710
Created by
admin on Fri Dec 15 17:52:07 GMT 2023 , Edited by admin on Fri Dec 15 17:52:07 GMT 2023
|
PRIMARY | |||
|
5511
Created by
admin on Fri Dec 15 17:52:07 GMT 2023 , Edited by admin on Fri Dec 15 17:52:07 GMT 2023
|
PRIMARY | |||
|
SU4B5T763F
Created by
admin on Fri Dec 15 17:52:07 GMT 2023 , Edited by admin on Fri Dec 15 17:52:07 GMT 2023
|
PRIMARY | |||
|
8494
Created by
admin on Fri Dec 15 17:52:07 GMT 2023 , Edited by admin on Fri Dec 15 17:52:07 GMT 2023
|
PRIMARY | |||
|
DTXSID1025722
Created by
admin on Fri Dec 15 17:52:07 GMT 2023 , Edited by admin on Fri Dec 15 17:52:07 GMT 2023
|
PRIMARY | |||
|
121-89-1
Created by
admin on Fri Dec 15 17:52:07 GMT 2023 , Edited by admin on Fri Dec 15 17:52:07 GMT 2023
|
PRIMARY | |||
|
204-504-3
Created by
admin on Fri Dec 15 17:52:07 GMT 2023 , Edited by admin on Fri Dec 15 17:52:07 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD
