2-Bromoethyl methyl ether - ≥95%(GC), stabilized with 30% NaOH solution , CAS No.6482-24-2

CAS: 6482-24-2 Cat. No.: B139139 Formula: BrCH₂CH₂OCH₃ Peso molecolare: 138.99 Beilstein Registry Number: 1(1)171 Numero EC: 229-339-4

GRADE & PURITY ≥95%(GC), stabilized with 30% NaOH solution

Synonyms

InChI=1/C3H7BrO/c1-5-3-2-4/h2-3H2,1H3 | BCP24711 | methoxy ethyl bromide | QMC9NTS6GR | 2-bromo-1-methoxyethane | Purasorb L | UNII-QMC9NTS6GR | 2-bromethyl methyl ether | 2- Methoxyethyl bromide | 2 -methoxyethyl bromide | 2-(methoxy)ethyl bromide | brom

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Panoramica

Kinetics of potassium iodide exchange reaction with 2-bromoethyl methyl ether in acetone at 15 and 25°C has been investigated
2-Bromoethyl methyl ether has been used as starting reagent in the synthesis of 1-bromo-4-(2-methoxyethox?y)benzene and 1-bromo-4-[(2-methoxyetho?xy)methyl]benzene

Specifications

Sinonimi

InChI=1/C3H7BrO/c1-5-3-2-4/h2-3H2,1H3 | BCP24711 | methoxy ethyl bromide | QMC9NTS6GR | 2-bromo-1-methoxyethane | Purasorb L | UNII-QMC9NTS6GR | 2-bromethyl methyl ether | 2- Methoxyethyl bromide | 2 -methoxyethyl bromide | 2-(methoxy)ethyl bromide | brom

Specifiche e purezza

≥95%(GC), stabilized with 30% NaOH solution

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Argon charged

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥95%(GC)

Nomi e identificatori

• Pubchem Sid: 504755488
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504755488
• Sorrisi canonici: COCCBr
• IUPAC Name: 1-bromo-2-methoxyethane
• InChIKey: YZUPZGFPHUVJKC-UHFFFAOYSA-N
• INCHI: 1S/C3H7BrO/c1-5-3-2-4/h2-3H2,1H3
• Isomeri SMILES: COCCBr
• WGK Germania: 3
• Peso molecolare: 138.99
• Beilstein: 1(1)171
• Reaxy-Rn: 773654
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=773654&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Ethers

• 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

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Proprietà chimiche e fisiche

• Solubilità: Soluble in water.14,4 g/L at 25°C
• Sensibilità: air & heat sensitive
• Indice di rifrazione: 1.448
• Punto di infiammabilità (°F): 82.4 °F
• Punto di infiammabilità (°C): 28 °C
• Punto di ebollizione (°C): 40-41 °C/66 mmHg
• Peso molecolare: 138.990 g/mol
• XLogP3: 0.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 137.968 Da
• Monoisotopic Mass: 137.968 Da
• Topological Polar Surface Area: 9.200 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 16.400
• 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

Riferimenti

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. Puxiang Yan, Haiyong Wang, Yuhe Liao, Chenguang Wang.  (2023)  Synthesis of renewable diesel and jet fuels from bio-based furanics via hydroxyalkylation/alkylation (HAA) over SO42-/TiO2 and hydrodeoxygenation (HDO) reactions.  FUEL,      [PMID:] [10.1016/j.fuel.2023.127685]

3. Weidong Lu, Zihao Xu, Meiyuan Li, Youheng Ma, Zijun Xiao.  (2022)  Deep eutectic solvent (DES) assisted deacidification of acidic oil and retaining catalyst activity: Variables optimization and catalyst characterization.  INDUSTRIAL CROPS AND PRODUCTS,      [PMID:] [10.1016/j.indcrop.2022.114990]

4. Jiayun Shi, Taishan Wang, Jie Han, Yao Liang, Yujia Tong, Weixing Li.  (2021)  Fabrication of MWCNTS-functionalized SA pervaporation composite membranes to enhance esterification.  JOURNAL OF APPLIED POLYMER SCIENCE,  139  (5): (51573).  [PMID:] [10.1002/app.51573]

5. Maliang Zhang, Yu Gao, Yuxin Zhang, Mengen Zhang, Yuan Gao, Bowen Cheng, Zhenhuan Li.  (2021)  Preparation and properties of polyphenylene sulfide/oxidized-polyphenylene sulfide composite membranes.  REACTIVE & FUNCTIONAL POLYMERS,      [PMID:] [10.1016/j.reactfunctpolym.2021.104842]

6. Chenhua Shu, Faying Lai, Feng Zhu, Dan Luo.  (2020)  Optimal extractive and reductive desulfurization process using sodium borohydride in situ generated via sodium metaborate electroreduction in ionic liquid.  Chemical Engineering and Processing-Process Intensification,      [PMID:] [10.1016/j.cep.2020.107869]

7. Hu Pan, Hu Li, Heng Zhang, Anping Wang, Duo Jin, Song Yang.  (2018)  Effective production of biodiesel from non-edible oil using facile synthesis of imidazolium salts-based Brønsted-Lewis solid acid and co-solvent.  ENERGY CONVERSION AND MANAGEMENT,      [PMID:] [10.1016/j.enconman.2018.04.061]

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11. Xianlong Liu, Yiting Zhao, Gewei Zhang, Chengxiang Shi, Lun Pan, Xiangwen Zhang, Ji-Jun Zou.  (2024)  Diels–Alder Reaction of Biofuran Derivatives and Cycloolefin for Directional Synthesis of Fused Ring Hydrocarbon High Density Jet Fuel.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.4c00808]

12. Wang Qiqi, Zhang Jingchun, Zhang Yilin, Song Shengjiao, Wang Guowei, Zhuang Linghua, Chen Xiaojun.  (2024)  Effect of ether introduction and ether chain length on electrochemical stability window feature of imidazolium ionic liquids with different anions: experimental and DFT studies.  IONICS,      [PMID:] [10.1007/s11581-024-05980-w]

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Domande frequenti

What is the purity of this product, and how is it determined?

This product is supplied at ≥95% purity, determined by gas chromatography (GC). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at 2–8 °C under argon. It is supplied under an argon blanket; reseal under inert gas after each use.

How is this product shipped?

This product ships chilled on wet ice. Unpack on arrival and transfer it to the storage condition stated above.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 6482-24-2, the molecular formula is C3H7BrO, and the molecular weight is 138.99 g/mol. InChIKey YZUPZGFPHUVJKC-UHFFFAOYSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.