(5-Bromo-2-methoxyphenyl)-2,3-
dihydro-1H-naphtho1.8-de1.3.2diazaborinine 927384-45-0 **科研现货速达** HPLC 随货提供COA、HPLC谱图、MS谱图，NMR图谱等，详细联系客服。用于LC-MS/MS定量分析，代谢组学、质谱，药代动力学等- 询价
- sogestandard
- 进口
- SGS-SR-103931
- 2026年07月03日
企业认证
相关产品推荐更多 >
(Fmoc-amino)cyclopropanecarboxylicacid 126705-22-4 **科研现货速达** HPLC 随货提供COA、HPLC谱图、MS谱图，NMR图谱等，详细联系客服。用于LC-MS/MS定量分析，代谢组学、质谱，药代动力学等
询价(1-naphthyl)propionic acid 775280-91-6 **科研现货速达** HPLC 随货提供COA、HPLC谱图、MS谱图，NMR图谱等，详细联系客服。用于LC-MS/MS定量分析，代谢组学、质谱，药代动力学等
询价
β-生育三烯醇 beta-Tocotrienol 490-23-3 **科研现货速达** ≥98% HPLC 随货提供COA、HPLC谱图、MS谱图，NMR图谱等，详细联系客服。用于LC-MS/MS定量分析，代谢组学、质谱，药代动力学等
询价![6-氯咪唑[1,2-b]吡啶嗪HCl 6-Chloroimidazo1,2-bpyridazineHCl 13493-79-3 **科研现货速达** ≥98% HPLC 随货提供COA、HPLC谱图、MS谱图，NMR图谱等，详细联系客服。用于LC-MS/MS定量分析，代谢组学、质谱，药代动力学等](https://img1.dxycdn.com/p/s14/2025/0809/216/6505860230306904591.jpg!wh200)
6-氯咪唑[1,2-b]吡啶嗪HCl 6-Chloroimidazo1,2-bpyridazineHCl 13493-79-3 **科研现货速达** ≥98% HPLC 随货提供COA、HPLC谱图、MS谱图，NMR图谱等，详细联系客服。用于LC-MS/MS定量分析，代谢组学、质谱，药代动力学等
询价
MitoTEMPOL,MitoTEMPOL,1101113-39-6,**科研现货速达** HPLC 随货提供COA、HPLC谱图、MS谱图，NMR图谱等，详细联系客服。用于LC-MS/MS定量分析，代谢组学、质谱，药代动力学等
询价
万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
- 英文名：
2-(5-Bromo-2-methoxyphenyl)-2,3-dihydro-1H-naphtho1.8-de1.3.2diazaborinine
- 库存：
999
- 供应商：
智溯科ZSK
- CAS号：
927384-45-0
- 规格：
10mg///100mg///200mg
风险提示：丁香通仅作为第三方平台，为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全，合理判断，谨慎选购商品，商家和用户对交易行为负责。对于医疗器械类产品，请先查证核实企业经营资质和医疗器械产品注册证情况。
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
技术资料暂无技术资料 索取技术资料
