≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Description
1-Bromo-2-(2-methoxyethoxy)ethane can be used in the synthesis of 1,4-diketo-3,6-diphenylpyrrolo[3,4-c]pyrrole(DPP)derivatives, which are stable and efficient pigments for two-photon excited fluorescence microscopy. It can also be used in the synthesis of a squarine dye, which exhibits a selective fluorogenic response towards zinc cation.
| Sorrisi canonici | COCCOCCBr |
|---|---|
| IUPAC Name | 1-(2-bromoethoxy)-2-methoxyethane |
| InChIKey | HUXJXNSHCKHFIL-UHFFFAOYSA-N |
| INCHI | 1S/C5H11BrO2/c1-7-4-5-8-3-2-6/h2-5H2,1H3 |
| Isomeri SMILES | COCCOCCBr |
| WGK Germania | 3 |
| Peso molecolare | 183.05 |
| Reaxy-Rn | 2069579 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2069579&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Classe | Organooxygen compounds |
| Subclass | Ethers |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Dialkyl ethers |
| Alternative Parents | Organobromides Hydrocarbon derivatives Alkyl bromides |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Dialkyl ether - Hydrocarbon derivative - Organobromide - Organohalogen compound - Alkyl halide - Alkyl bromide - Aliphatic acyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as dialkyl ethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups. |
| External Descriptors | Not available |
| Indice di rifrazione | 1.4540 to 1.4590 |
|---|---|
| Punto di infiammabilità (°F) | 154.4 °F |
| Punto di infiammabilità (°C) | 68 °C |
| Punto di ebollizione (°C) | 156 °C |
| Peso molecolare | 183.040 g/mol |
| XLogP3 | 0.500 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 5 |
| Exact Mass | 181.994 Da |
| Monoisotopic Mass | 181.994 Da |
| Topological Polar Surface Area | 18.500 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 41.400 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Liang Ren, Jianxin Chen, Jian Han, Jinsheng Liang, Hong Wu. (2023) Anti-scaling covalent organic framework membranes with custom-tailored nanochannels for efficient lithium extraction. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2023.142112] |
| 2. Wei Sun, Yingxue Zhang, Zhi Zeng, Najun Li, Qingfeng Xu, Hua Li, Dongyun Chen, Jianmei Lu. (2026) Alkoxy-functionalized covalent organic polymer membranes for high-performance dye/salt separation. SEPARATION AND PURIFICATION TECHNOLOGY, [PMID:] [10.1016/j.seppur.2026.139729] |
