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About This Item
Linear Formula:
C6H3FICOOH
CAS Number:
Molecular Weight:
266.01
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
form
solid
mp
164-168 °C (lit.)
SMILES string
OC(=O)c1cc(I)ccc1F
InChI
1S/C7H4FIO2/c8-6-2-1-4(9)3-5(6)7(10)11/h1-3H,(H,10,11)
InChI key
QNNJHBNTHVHALE-UHFFFAOYSA-N
Application
2-Fluoro-5-iodobenzoic acid may be used in the preparation of 1-N-ethyl 6-iodoquinolonic acid and 1-N-cyclopropyl 6-iodoquinolonic acid. It may also be used as a precursor for the generation of electron transfer dissociation (ETD) reagents.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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’.
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Find documentation for the products that you have recently purchased in the Document Library.
Synthesis and biological activity of 4 ″-O-acyl derivatives of 14-and 15-membered macrolides linked to ω-quinolone-carboxylic unit.
Skugor MM, et al.
Bioorganic & Medicinal Chemistry, 18(17), 6547-6558 (2010)
Electron-transfer reagent anion formation via electrospray ionization and collision-induced dissociation.
Huang TY, et al.
Analytical Chemistry, 78(21), 7387-7391 (2006)
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