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关于此项目
线性分子式:
BrC6H3(OCH3)2
化学文摘社编号:
分子量:
217.06
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
solid
Quality Level
assay
97%
form
solid
mp
62-66 °C (lit.)
functional group
bromo
SMILES string
COc1cc(Br)cc(OC)c1
InChI
1S/C8H9BrO2/c1-10-7-3-6(9)4-8(5-7)11-2/h3-5H,1-2H3
InChI key
KRWRFIMBWRVMKE-UHFFFAOYSA-N
General description
以 1,3-二甲氧基苯为原料,通过铱催化芳香硼化反应合成 1-溴-3,5-二甲氧基苯。
Application
1-溴-3,5-二甲氧基苯可用于合成以下物质:
- 双 -[二-(3,5-二甲氧基苯基)甲基环戊二烯基] 二氯化钛 (IV),{ η 5 - C 5 H 4 -CH-[C 6 H 4 -(OCH 3 ) 2 2 ) 2 TiCl 2 可作为抗癌药物,通过多步反应工艺获得
- 5-溴-苯-1,3-二醇通过三溴化硼 (BBr 3 ) 去甲基化
- 硝化反应生成 1-溴-3,5-二甲氧基-2-硝基苯
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
"Diarylmethyl substituted titanocenes: promising anti-cancer drugs"
Pampillon C, et al.
Polyhedron, 25(10), 2101-2108 (2006)
"Photoswitching azo compounds in vivo with red light"
Samanta S, et al.
Journal of the American Chemical Society, 135(26), 9777- 9784 (2013)
"Novel CYP17 inhibitors: Synthesis, biological evaluation, structure?activity relationships and modelling of methoxy-and hydroxy-substituted methyleneimidazolyl biphenyls"
Hille.U, et al.
European Journal of Medicinal Chemistry, 44(7), 2765-2775 (2009)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 569313-25G | 04061832597096 |
| 569313-5G | 04061832280301 |