2-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene(CAS番号:503070-57-3)
基本情報
![2-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene 2-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene](/structs/503/503070-57-3-bc25.webp)
CAS番号
503070-57-3
分子式
C15H21BrCl2O2
分子量
384.14 g/mol
Quick Actions
基本的な物理特性
沸点
420.8±45.0°C at 760 mmHg
密度
1.335±0.06 g/cm3 (20 ºC 760 Torr),
溶解度
Insuluble (5.0E-3 g/L) (25 ºC),
安全情報
安全情報を表示危険性の表示
H302
同義語と参考文献
英語
- 2-((2-((6-Bromohexyl)oxy)ethoxy)methyl)-1,3-dichlorobenzene
- 2-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene
- Benzene, 2-[[2-[(6-bromohexyl)oxy]ethoxy]methyl]-1,3-dichloro-
- Benzene, 2-[[2-[(6-broMohexyl)oxy]ethoxy]Methyl]-1,3-dichloro
- 2-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene,Benzene
- AK342713
- 2-[[2-[(6-Bromohexyl)oxy]ethoxy]methyl]-1,3-dichlorobenzene
- 2-({2-[(6-Bromohexyl)oxy]ethoxy}methyl)-1,3-dichlorobenzene
- benzene,
- Vilanterol intermediate
- AKLUHFHHUBIDQA-UHFFFAOYSA-N
- BCP17123
- 2-[[2-[(6-broMohexyl)oxy]ethoxy
- SY046035
- 2-((2-((6-bromohexyl)oxy)ethoxy)methyl)-1,3-dichlorobenzene
- DS-12378
- benzene,2-((2-((6-bromohexyl)oxy)ethoxy)methyl)-1,3-dichloro-
- 2-[2-(6-bromo-hexyloxy)-ethoxymethyl]-1,3-dichloro-benzene
- SCHEMBL924842
- C15H21BrCl2O2
- MFCD21337362
- 2-[2-(6-Bromo-hexyloxy)-ethoxvmethyl]-1,3-dichloro-benzene
- AMY30043
- F11658
- 2-[2-(6-bromohexoxy)ethoxymethyl]-1,3-dichlorobenzene
- Benzene, 2-[[2-[(6-bromohexyl)oxy]ethoxy]methyl]-1,3-dichloro-
- 503070-57-3
- AC-30864
- 4UXW94FP9H
- 2-(2-(6-bromohexyloxy)ethoxymethyl)-1,3-dichlorobenzene
- AKOS027250612
- CS-M2591
MDL_Number
MFCD21337362
CAS番号
503070-57-3
サプライヤー情報
サプライヤー名 | 会員レベル | 認証状況 | 主要カテゴリー | 最小注文数量 | アクション |
---|---|---|---|---|---|
関連論文
Ether-functionalization of monoethanolamine (MEA) for reversible CO2 capture under solvent-free conditions with high-capacity and low-viscosity
An-Hua Liu, Jie-Jie Li, Bai-Hao Ren, Xin-Ru Sha, He Jiang, Xiao-Bing Lu
DOI: 10.1039/C9SE00756C
Non-aqueous neptunium and plutonium redox behaviour in THF – access to a rare Np(iii) synthetic precursor
Nickolas H. Anderson, Suzanne C. Bart, Andrew J. Gaunt, Brian L. Scott
DOI: 10.1039/C8CC02611D
Visible light-driven cross-coupling reactions of alkyl halides with phenylacetylene derivatives for C(sp3)–C(sp) bond formation catalyzed by a B12 complex
Li Chen, Yohei Kametani, Kenji Imamura, Tsukasa Abe, Yoshihito Shiota, Kazunari Yoshizawa, Yoshio Hisaeda, Hisashi Shimakoshi
DOI: 10.1039/C9CC06185A
Heterogeneous toroidal spiral particles for islet encapsulation
Paola Leon Plata, Maryam Zaroudi, Chun-Yin Lee, Colin Foster, Ludwig C. Nitsche, Peter D. Rios, Yong Wang, Jose Oberholzer
DOI: 10.1039/D0BM02082F
Nickel-containing N-doped carbon as effective electrocatalysts for the reduction of CO2 to CO in a continuous-flow electrolyzer
Bert De Mot, Daniel Choukroun, Chen Li, Annick Hubin, Sara Bals, Jonas Hereijgers
DOI: 10.1039/C9SE00814D
Chemoproteomics-based target profiling of sinomenine reveals multiple protein regulators of inflammation
Lianguo Chen, Hong-jian Wang, Teng-fei Ji, Chong-Jing Zhang
DOI: 10.1039/D1CC01522B
Life cycle assessment of plasma-assisted ethylene production from rich-in-methane gas streams
Evangelos Delikonstantis, Elorri Igos, Michael Augustinus, Enrico Benetto
DOI: 10.1039/C9SE00736A
Permselective ion electrosorption of subnanometer pores at high molar strength enables capacitive deionization of saline water
Luca Cervini
DOI: 10.1039/C9SE00996E
Redox responsive Pluronic micelle mediated delivery of functional siRNA: a modular nano-assembly for targeted delivery
Sandeep Kadekar, Ganesh N. Nawale, Vadim Le Joncour, Pirjo Laakkonen, Jöns Hilborn, Oommen P. Varghese, Oommen P. Oommen
DOI: 10.1039/D1BM00428J
Synthesis and hydrogen evolving catalysis of a panchromatic photochemical molecular device
Johannes Habermehl, Djawed Nauroozi, Miłosz Martynow, Yury E. Vilk, Radim Beranek, Julien Guthmuller, Sven Rau
DOI: 10.1039/C9SE00304E