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Merck
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重要文件

143219

Sigma-Aldrich

4-溴苯肼 盐酸盐

99%

同義詞:

1-(4-Bromophenyl)hydrazine hydrochloride, 2-(4-Bromophenyl)hydrazinium chloride, 4-Bromophenylhydrazine monohydrochloride, p-Bromophenylhydrazine monohydrochloride

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About This Item

線性公式:
BrC6H4NHNH2·HCl
CAS號碼:
分子量::
223.50
Beilstein:
3565838
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

99%

形狀

powder

mp

220-230 °C (dec.) (lit.)

官能基

bromo
hydrazine

SMILES 字串

Cl.NNc1ccc(Br)cc1

InChI

1S/C6H7BrN2.ClH/c7-5-1-3-6(9-8)4-2-5;/h1-4,9H,8H2;1H

InChI 密鑰

RGGOWBBBHWTTRE-UHFFFAOYSA-N

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應用

4-Bromophenylhydrazine hydrochloride was used as reagent in the synthesis of:
  • acylsulfonamides and acylsulfamides
  • 9-bromo-2-ethenyl-7,12-dihydroindolo[3,2-d][1]benzazepin-6(5H)-one

象形圖

Corrosion

訊號詞

Danger

危險聲明

危險分類

Skin Corr. 1B

儲存類別代碼

8A - Combustible corrosive hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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分析證明 (COA)

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Michael P Winters et al.
Bioorganic & medicinal chemistry letters, 18(6), 1926-1930 (2008-03-01)
A series of novel acylsulfonamide, acylsulfamide, and sulfonylurea bioisosteres of carboxylic acids were prepared as CXCR2 antagonists. Structure-activity relationships are reported for these series. One potent orally bioavailable inhibitor had excellent PK properties and was active in a lung injury
Xu Xie et al.
European journal of medicinal chemistry, 40(7), 655-661 (2005-06-07)
The introduction of side chains bearing epoxide motifs into the molecular scaffold of kenpaullone and 9-trifluoromethylpaullone led to improved antiproliferative activity of the novel derivatives for human tumor cell lines. The syntheses were accomplished applying Stille coupling for the introduction
Siva Doddi et al.
Journal of fluorescence, 26(6), 1939-1949 (2016-11-01)
We report the synthesis and characterization of a new fluorescent dyad SP-DPP-SP(9) via efficient palladium-catalyzed Sonogashira coupling of prop-2-yn-1-yl 3-(3',3'dimethyl-6-nitrospiro[chromene-2,2'-indolin]-1'-yl)propanoatespiropyran, SP(8), a well known photochromic accepter, with 3,6-bis(5-bromothiophen-2-yl)-2,5-bis((R)-2-ethylhexyl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione, DPP(4), a highly fluorescent donor. Under visible light exposure the SP unit
Ilkoo Noh et al.
Advanced science (Weinheim, Baden-Wurttemberg, Germany), 5(3), 1700481-1700481 (2018-03-30)
A noninvasive and selective therapy, photodynamic therapy (PDT) is widely researched in clinical fields; however, the lower efficiency of PDT can induce unexpected side effects. Mitochondria are extensively researched as target sites to maximize PDT effects because they play crucial

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