569313
1-溴-3,5-二甲氧基苯
97%
别名:
3,5-二甲氧基-1-溴苯, 3,5-二甲氧基溴苯, 3,5-二甲氧基苯基溴, 5-溴-1,2,3-二甲基苯
登录 查看组织和合同定价。
选择尺寸
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:
产品名称
1-溴-3,5-二甲氧基苯, 97%
InChI
1S/C8H9BrO2/c1-10-7-3-6(9)4-8(5-7)11-2/h3-5H,1-2H3
SMILES string
COc1cc(Br)cc(OC)c1
InChI key
KRWRFIMBWRVMKE-UHFFFAOYSA-N
assay
97%
form
solid
mp
62-66 °C (lit.)
functional group
bromo
Quality Level
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
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。
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)
"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)
"Photoswitching azo compounds in vivo with red light"
Samanta S, et al.
Journal of the American Chemical Society, 135(26), 9777- 9784 (2013)
"Diarylmethyl substituted titanocenes: promising anti-cancer drugs"
Pampillon C, et al.
Polyhedron, 25(10), 2101-2108 (2006)
Takashi Iijima et al.
Bioscience, biotechnology, and biochemistry, 73(11), 2547-2548 (2009-11-10)
An efficient synthesis of tri-O-methylated resveratrol is presented using an advanced Heck reaction promoted by Pd(dba)(2) in the presence of P(t-Bu)(3).
Ryan T Pekarek et al.
Journal of the American Chemical Society, 140(41), 13223-13232 (2018-10-04)
The design and fabrication of stable and efficient photoelectrochemical devices requires the use of multifunctional structures with complex heterojunctions composed of semiconducting, protecting, and catalytic layers. Understanding charge transport across such devices is challenging due to the interplay of bulk
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持