491748
4-(溴甲基)吡啶 氢溴酸盐
97%
别名:
4-溴甲基吡啶单氢溴酸盐, 4-甲基吡啶溴氢溴酸盐, （4-吡啶）甲基溴氢溴酸盐
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关于此项目
经验公式（希尔记法）:
C6H6BrN · HBr
化学文摘社编号:
分子量:
252.93
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
产品名称
4-(溴甲基)吡啶 氢溴酸盐, 97%
InChI
1S/C6H6BrN.BrH/c7-5-6-1-3-8-4-2-6;/h1-4H,5H2;1H
SMILES string
Br[H].BrCc1ccncc1
InChI key
VAJUUDUWDNCECT-UHFFFAOYSA-N
assay
97%
mp
189-192 °C (lit.)
functional group
bromo
Quality Level
Application
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
General description
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。
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
Luca Simeone et al.
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Novel thymidine- or uridine-based nucleolipids, containing one hydrophilic oligo(ethylene glycol) chain and one or two oleic acid residues (called ToThy, HoThy and DoHu), have been synthesized with the aim to develop bio-compatible nanocarriers for drug delivery and/or produce pro-drugs. Microstructural
Cristiane F da Costa et al.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 63(1), 40-42 (2008-02-12)
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
Photoinduced electron transfer in supramolecular complexes of a p-extended viologen with porphyrin monomer and dimer.
Fukuzumi S, et al.
Royal Society of Chemistry Advances, 2(9), 3741-3747 (2012)
Saleh Ihmaid et al.
European journal of medicinal chemistry, 45(11), 4934-4946 (2010-08-31)
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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