추천 제품
분석
99%
양식
liquid
refractive index
n20/D 1.5072 (lit.)
bp
50-52 °C/0.15 mmHg (lit.)
density
1.061 g/mL at 25 °C (lit.)
작용기
amine
fluoro
SMILES string
NCCc1ccc(F)cc1
InChI
1S/C8H10FN/c9-8-3-1-7(2-4-8)5-6-10/h1-4H,5-6,10H2
InChI key
CKLFJWXRWIQYOC-UHFFFAOYSA-N
유전자 정보
human ... AOC3(8639)
mouse ... Aoc3(11754)
애플리케이션
4-Fluorophenethylamine may be employed as nucleophile in the synthesis of 2-amino-4-arylpyrimidine derivatives.[1] It is suitable for use in the preparation of ortho-metalated primary phenethylamines having electron-releasing and electron-withdrawing groups on the aromatic ring, leading to complexes containing six membered palladacycles.[2]
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Oral - Skin Corr. 1B
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
Flash Point (°F)
174.2 °F - closed cup
Flash Point (°C)
79 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
이미 열람한 고객
Mitra Matloobi et al.
Journal of combinatorial chemistry, 9(2), 275-284 (2007-03-14)
An efficient and rapid microwave-assisted solution-phase method for the synthesis of 2-amino-4-arylpyrimidine-5-carboxylic acid derivatives has been developed. The five-step linear protocol involves an initial Biginelli multicomponent reaction leading to dihydropyrimidine-2-thiones which are subsequently S-alkylated with methyl iodide. The resulting 2-methylthiodihydropyrimidines
Ortho-metalated primary amines. 6.1 The first synthesis of six-membered palladacycles from primary amines containing electron-withdrawing substituents: end of the limiting rules of Cope and Friedrich on cyclopalladation of benzyl-and phenethylamines.
Vicente J, et al.
Organometallics, 22(26), 5513-5517 (2003)
Tianqi Niu et al.
Nano letters, 19(10), 7181-7190 (2019-09-04)
Perovskite solar cells based on two-dimensional/three-dimensional (2D/3D) hierarchical structure have attracted significant attention in recent years due to their promising photovoltaic performance and stability. However, obtaining a detailed understanding of interfacial mechanism at the 2D/3D heterojunction, for example, the ligand-chemistry-dependent
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