- ¥5754.90 - 18508.90
- 阿拉丁
- B1270600
- 上海
- 2026年05月12日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
期货
- 英文名：
2-Bromo-4-(3-methoxyphenyl)-1-butene
- CAS号：
104997-02-6
- 供应商：
上海阿拉丁生化科技股份有限公司
- 保存条件：
室温；常规运输
- 规格：
B1270600-1g/B1270600-2g/B1270600-5g
| 规格： | B1270600-1g | 产品价格： | ¥5754.90 |
|---|---|---|---|
| 规格： | B1270600-2g | 产品价格： | ¥7756.90 |
| 规格： | B1270600-5g | 产品价格： | ¥18508.90 |
中文名：2-Bromo-4-(3-methoxyphenyl)-1-butene
英文名：2-Bromo-4-(3-methoxyphenyl)-1-butene
纯度：≥95%
货号：B1270600
Cas号：104997-02-6
存储温度：室温
运输条件：常规运输
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文献和实验A Historical Overview of Bromo-Substituted DNA and Sister Chromatid Differentiation
The thymidine analogue 5-bromo-2′-deoxyuridine (BrdU) has been widely used to make sister chromatid differentiation (SCD) evident in metaphase chromosomes of cells grown for two cycles in BrdU and, thus, containing varying
, or other biologically active molecules. In this chapter, we present a technique, which allows identification of specific DNA sequences by fluorescence in situ hybridization (FISH) and simultaneously analyses the incorporation of a thymidine analogue, 5-bromo
Natural Product Chemistry in Action: The Synthesis of Melatonin Metabolites K1 and K2
melatonin, the kynurenamines N1-acetyl-N2 -formyl-5-methoxykynurenine (K1 ) and N -acetyl-5-methoxykynurenamine (K2 ). The four key synthetic transformations involve (a) conversion of 4-methoxy aniline into the tert -butyl (4-methoxyphenyl)carbamate, (b
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