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1)  3,5-dimethoxybromobenzene
3,5-二甲氧基溴苯
1.
Methods Adipostatin A was synthesized from 3,5-dimethoxybromobenzene through three steps: metallation with Mg,coupling,with(Z)-1-bromo-8-pentadecane in the presence of Li2CuCl4-THF,demethylation with MeMgI.
方法以3,5-二甲氧基溴苯为原料,经金属化、偶联、脱甲基化反应制得Adipostatin A。
2.
Methods Olivetol was synthesized from 3,5-dimethoxybromobenzene through metallation,coupling,demethylation.
方法以3,5-二甲氧基溴苯为原料,经金属化、耦联、脱甲基化反应制得Olivetol。
3.
Irisquinone was synthesized from 3,5-dimethoxybromobenzene through four steps,namely metallation,coupling,demethylation and Teuber oxidation.
3,5-二甲氧基溴苯为原料,经金属化、偶联、脱甲基化、Teuber氧化反应制得标题化合物。
2)  4-bromo-3,5-dimethoxybenzaldehyde
4-溴-3,5-二甲氧基苯甲醛
1.
Synthesis and structural characterization of 4-bromo-3,5-dimethoxybenzaldehyde;
4-溴-3,5-二甲氧基苯甲醛的合成与表征
3)  3,5-Bis(bromomethyl)toluene
3,5-二溴甲基甲苯
4)  5-Bromo-m-xylene
3,5-二甲基溴苯
5)  1-bromo-3,5-dimethyl-benzene
1-溴-3,5-二甲基苯
6)  3,5-dimethoxybenzyl bromide
3,5-二甲氧基苄溴
1.
Synthesis of 3,5-dimethoxybenzyl bromide;
3,5-二甲氧基苄溴的合成
2.
Some new stilbenes were synthesized from 3,5-dimethoxybenzyl bromide and sodium cyanide as starting materials via cyaniding,hydrolysis,condensation and demethylation The structures of all products were confirmed by IR,1HNMR,MS spectra and elementary analysis.
以3,5-二甲氧基苄溴和氰化钠为起始原料,经过氰化、水解、缩合、脱甲基等反应制备出几种新的芪类化合物,其结构经IR、1HNMR、MS和元素分析确证,并讨论了影响反应的因素。
3.
OBJECTIVE To synthesize 3,5-dimethoxybenzyl bromide METHODS 3,5-dimethoxybenzoic acid was reducted with NaBH4/I2, to obtain 3,5-dimethoxybenzyl alcohol, then brominated with 40% HBr.
目的合成药物中间体3,5-二甲氧基苄溴。
补充资料:2,4-二甲氧基溴苯
分子式:C8H9BrO2
分子量:217.06
CAS号:17715-69-4

性质:密度1.507。熔点25-26°C。沸点153-155°C (18 mmHg)。折射率1.5718-1.5738。闪点109°C。水溶性insoluble。

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