추천 제품
Quality Level
분석
97%
형태
solid
mp
47-49 °C (lit.)
작용기
fluoro
nitrile
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
일반 설명
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.
애플리케이션
2,4-Difluorobenzonitrile has been used in the synthesis of:
- 2-methylsulfonyl-4-fluorobenzylamine
- fluoro-3-amino-1,2-benzisoxazoles
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
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
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
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.
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