All Photos(1)
About This Item
Linear Formula:
F2C6H3CN
CAS Number:
Molecular Weight:
139.10
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
97%
form
solid
mp
47-49 °C (lit.)
SMILES string
Fc1ccc(C#N)c(F)c1
InChI
1S/C7H3F2N/c8-6-2-1-5(4-10)7(9)3-6/h1-3H
InChI key
LJFDXXUKKMEQKE-UHFFFAOYSA-N
General description
2,4-Difluorobenzonitrile undergoes polycondensation with Bisphenol A and matrix-assisted laser desorption/time-of-flight mass spectra revealed a quantitative formation of cyclic oligoethers and polyethers.
Application
2,4-Difluorobenzonitrile has been used in the synthesis of:
- 2-methylsulfonyl-4-fluorobenzylamine
- fluoro-3-amino-1,2-benzisoxazoles
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - 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)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
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’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Macrocycles. XXVIII. Cyclic poly (benzonitrile ether) s derived from bisphenol A.
Kricheldorf HR, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 41(23), 3838-3846 (2003)
Practical Synthesis of 4-Fluoro-2-(methylthio) benzylamine and the Corresponding Sulfone and Sulfonamide.
Perlow DS, et al.
Synthetic Communications, 37(11), 1887-1897 (2007)
S D Lepore et al.
The Journal of organic chemistry, 65(10), 2924-2932 (2000-05-18)
Further exploration of the scope of our solid-phase method for the synthesis of 3-aminobenzisoxazoles (using the Kaiser oxime resin 1) is described. The effects of base, leaving group, and solvent on the nucleophilic aromatic substitution based resin-loading reaction are discussed.
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