All Photos(1)
About This Item
Linear Formula:
I2C6H3CO2H
CAS Number:
Molecular Weight:
373.91
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
97%
mp
183-187 °C (lit.)
SMILES string
OC(=O)c1cc(I)ccc1I
InChI
1S/C7H4I2O2/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3H,(H,10,11)
InChI key
NSKPFWAAYDFCFS-UHFFFAOYSA-N
Related Categories
Application
2,5-Diiodobenzoic acid was used for detection and responses of divergent compounds which are strong electron absorbers by gas chromatography with electron capture detection.
Biochem/physiol Actions
2,5-Diiodobenzoic acid forms 1:1 complex with cycloheptaamylose. It undergoes palladium-catalyzed coupling reaction with terminal alkynes.
Signal Word
Warning
Hazard Statements
Hazard Classifications
Acute Tox. 4 Oral
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Attogram-level detection and relative sensitivity of strong electrophores by gas chromatography with electron capture detection.
Corkill JA, et al
Analytical Chemistry, 54(3), 481-485 (1982)
Highly regioselective palladium-catalyzed condensation of terminal acetylenes with 2, 5-diiodobenzoic acid.
Balavoine F, et al.
Tetrahedron Letters, 40(48), 8351-8354 (1999)
The crystal structure of a complex of cycloheptaamylose with 2,5-diiodobenzoic acid.
J A Hamilton et al.
Biochemical and biophysical research communications, 73(3), 659-664 (1976-12-06)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service