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品質等級
化驗
97%
mp
189-192 °C (lit.)
SMILES 字串
Br[H].BrCc1ccncc1
InChI
1S/C6H6BrN.BrH/c7-5-6-1-3-8-4-2-6;/h1-4H,5H2;1H
InChI 密鑰
VAJUUDUWDNCECT-UHFFFAOYSA-N
一般說明
4-(溴甲基)吡啶氢溴酸盐是取代的吡啶。它与 1,2-乙二胺和 1,3-丙二胺反应生成相应的二胺。
應用
4-(溴甲基)吡啶氢溴酸盐可用于制备:
- 3-(4-吡啶基甲基)-2′,3′-二-O-油基-5′-O-(4,4′-二甲氧基三苯基甲基)尿苷
- 3-(4-吡啶基甲基)-3′-O-油基-5′-O-(4,4-二甲氧基三苯甲基)-胸苷
- 1,4-双(N-己基-4-吡啶)丁二烯二氯酸盐
- 2-吗啉-4-基-7-(吡啶-4-基甲氧基)-4H-1,3-苯并恶嗪-4-酮
- 8-甲基-2-吗啉-4-基-7-(吡啶-4-基甲氧基)-4H-1,3-苯并恶嗪-4-酮
- 2-吗啉-4-基-8-(吡啶-4-基甲氧基)-4H-1,3-苯并恶嗪-4-酮
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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We report in this work the preparation and the in vitro antileishmanial activity of a series of long chains N-monoalkylated diamines and two pyridinediamine derivatives. Several compounds, tested for their in vitro antiproliferative activity against Leishmania amazonensis and Leishmania chagasi
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A number of new 2-amino-[5, 6, 7 and 8]-O-substituted 1,3-benzoxazines, and 2-amino 8-methyl-7-O-substituted-1,3-benzoxazines were synthesized. Thirty one new compounds were tested for their effect on collagen induced platelet aggregation and it was found that the most active compounds were 8-methyl-2-morpholin-4-yl-7-(pyridin-3-ylmethoxy)-4H-1,3-benzoxazin-4-one
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