추천 제품
Quality Level
분석
98%
양식
solid
mp
51-53 °C (lit.)
작용기
bromo
SMILES string
Nc1cc(Br)ccc1Br
InChI
1S/C6H5Br2N/c7-4-1-2-5(8)6(9)3-4/h1-3H,9H2
InChI key
WRTAZRGRFBCKBU-UHFFFAOYSA-N
관련 카테고리
애플리케이션
2,5-Dibromoaniline was used in the synthesis of 2,4,5-tribromoaniline. It was also used as starting reagent in the regioselective synthesis of 2-(3,4-dimethoxyphenyl)-5-bromobenzothiazole.
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 - Skin Sens. 1 - 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, Faceshields, Gloves
이미 열람한 고객
Dalton transactions (Cambridge, England : 2003), 48(14), 4489-4494 (2019-03-13)
A new Eu-MOF was designed from an amino-functionalized ligand and Eu(iii) ions under solvothermal conditions. It is a highly porous, water-stable, and luminescent material, exhibiting pH sensing in the acidic range of pH = 7-3 with selective detection for Cd2+
Talanta, 206, 120179-120179 (2019-09-14)
In this work, the magnetic amino-functionalized microporous organic network composites (Fe3O4@MON-NH2) were rational designed and facile synthesized for magnetic solid phase extraction (MSPE) of endocrine disrupting chemicals (EDCs), followed by their analysis with high-performance liquid chromatography. The incorporation of amino
Induction of both cytochromes P-450 and P-448 by 2,3',4,4',5-pentabromobiphenyl, a component of fireMaster.
Biochemical and biophysical research communications, 92(1), 175-182 (1980-01-15)
Journal of chromatography. A, 1616, 460791-460791 (2019-12-24)
Microporous organic network (MON) is a promise class of functional materials in solid phase extraction (SPE). However, the previous MON-based SPE works are all focused on off-line mode. The inherent drawbacks of off-line SPE such as complicated operation steps and
Journal of medicinal chemistry, 49(1), 179-185 (2006-01-06)
A series of new 2-phenylbenzothiazoles has been synthesized on the basis of the discovery of the potent and selective in vitro antitumor properties of 2-(3,4-dimethoxyphenyl)-5-fluorobenzothiazole (8n; GW 610, NSC 721648). Synthesis of analogues substituted in the benzothiazole ring was achieved
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