Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H5IO2 |
| Molecular Weight | 248.0179 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=CC=C(I)C=C1
InChI
InChIKey=GHICCUXQJBDNRN-UHFFFAOYSA-N
InChI=1S/C7H5IO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,(H,9,10)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Oxidative cleavage of alkenes using an in situ generated iodonium ion with oxone as a terminal oxidant. | 2010-12-17 |
|
| Aqua-(2,2'-bipyridine-κN,N')bis-(4-iodo-benzoato-κO)copper(II). | 2010-11-10 |
|
| In-line coupling of two-phase single drop microextraction and large volume stacking using an electroosmotic flow pump in nonaqueous capillary electrophoresis. | 2009-09-11 |
|
| Synthesis and biological activity of a novel series of 6-substituted thieno[2,3-d]pyrimidine antifolate inhibitors of purine biosynthesis with selectivity for high affinity folate receptors over the reduced folate carrier and proton-coupled folate transporter for cellular entry. | 2009-05-14 |
|
| Growth inhibition mode of action of selected benzoic acid derivatives against the yeast Pichia anomala. | 2009-04 |
|
| On the selection of a tracer for PET imaging of HER2-expressing tumors: direct comparison of a 124I-labeled affibody molecule and trastuzumab in a murine xenograft model. | 2009-03 |
|
| Affibody molecules for epidermal growth factor receptor targeting in vivo: aspects of dimerization and labeling chemistry. | 2009-02 |
|
| Comparison of benzoate- and dodecaborate-based linkers for attachment of radioiodine to HER2-targeting Affibody ligand. | 2007-03 |
|
| On the solid state structure of 4-iodobenzoic acid. | 2005-03-24 |
|
| [Catalytic activity of butyrylcholinesterase in biodegradation of organic ammonium salts in vitro]. | 2004-03 |
|
| In vitro selectivity, in vivo biodistribution and tumour uptake of annexin V radiolabelled with a positron emitting radioisotope. | 2003-10-06 |
|
| Biodistribution of the chimeric monoclonal antibody U36 radioiodinated with a closo-dodecaborate-containing linker. Comparison with other radioiodination methods. | 2003-07-17 |
|
| Optimization of a convenient route to produce N-succinimidyl 4-radiodobenzoate for radioiodination of proteins. | 2003-06 |
|
| Radioiodination of proteins using prosthetic group: a convenient way to produce labelled proteins with in vivo stability. | 2002-11 |
|
| The use of mutants to discern the degradation pathway of 3,4'-dichlorobiphenyl in Pseudomonas acidovorans M3GY. | 2002-10-01 |
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
3773
Created by
admin on Mon Mar 31 19:52:57 GMT 2025 , Edited by admin on Mon Mar 31 19:52:57 GMT 2025
|
PRIMARY | |||
|
210-603-2
Created by
admin on Mon Mar 31 19:52:57 GMT 2025 , Edited by admin on Mon Mar 31 19:52:57 GMT 2025
|
PRIMARY | |||
|
IPO4LYQ1EN
Created by
admin on Mon Mar 31 19:52:57 GMT 2025 , Edited by admin on Mon Mar 31 19:52:57 GMT 2025
|
PRIMARY | |||
|
619-58-9
Created by
admin on Mon Mar 31 19:52:57 GMT 2025 , Edited by admin on Mon Mar 31 19:52:57 GMT 2025
|
PRIMARY | |||
|
176127
Created by
admin on Mon Mar 31 19:52:57 GMT 2025 , Edited by admin on Mon Mar 31 19:52:57 GMT 2025
|
PRIMARY | |||
|
DTXSID20862304
Created by
admin on Mon Mar 31 19:52:57 GMT 2025 , Edited by admin on Mon Mar 31 19:52:57 GMT 2025
|
PRIMARY | |||
|
12085
Created by
admin on Mon Mar 31 19:52:57 GMT 2025 , Edited by admin on Mon Mar 31 19:52:57 GMT 2025
|
PRIMARY |
SUBSTANCE RECORD
