1-(2-Bromoethoxy)-2-(2-methoxyethoxy)ethane - ≥97% , CAS No.72593-77-2

CAS: 72593-77-2 Cat. No.: B471551 Summenformel: C₇H₁₅BrO₃ Molekulargewicht: 227.1 EG-Nummer: 679-854-7

GRADE & PURITY ≥97%

Synonyms

1-bromo-2-(2-(2-methoxyethoxyl)ethoxy)ethane | 1-bromo-2-(2-(2-methoxyethoxyl)ethoxy)-ethane | Diethylene Glycol 2-Bromoethyl Methyl Ether | AS-44531 | A905818 | SCHEMBL2024399 | 1-(2-Bromoethoxy)-2-(2-methoxyethoxy)ethane, 97% | m-PEG3-bromide | SY055077

Storage

Store at 2-8°C,Protected from light,Argon charged

Shipped In

Wet ice

Application

227,228,229

Specifications

Synonyme

1-bromo-2-(2-(2-methoxyethoxyl)ethoxy)ethane | 1-bromo-2-(2-(2-methoxyethoxyl)ethoxy)-ethane | Diethylene Glycol 2-Bromoethyl Methyl Ether | AS-44531 | A905818 | SCHEMBL2024399 | 1-(2-Bromoethoxy)-2-(2-methoxyethoxy)ethane, 97% | m-PEG3-bromide | SY055077

Spezifikationen & Reinheit

≥97%

Storage

Store at 2-8°C,Protected from light,Argon charged

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Reinheit

≥97%

Namen und Kennungen

• Pubchem Sid: 488198380
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488198380
• Kanonisches Lächeln: COCCOCCOCCBr
• IUPAC Name: 1-[2-(2-bromoethoxy)ethoxy]-2-methoxyethane
• InChIKey: LCCCTXULXHJDLA-UHFFFAOYSA-N
• INCHI: 1S/C7H15BrO3/c1-9-4-5-11-7-6-10-3-2-8/h2-7H2,1H3
• Isomere SMILES: COCCOCCOCCBr
• Molekulargewicht: 227.1
• Reaxy-Rn: 2234078
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2234078&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Klasse: 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
• Beschreibung: 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

Chemische und physikalische Eigenschaften

• Empfindlichkeit: moisture sensitive；heat sensitive；air sensitive；light sensitive
• Brechungsindex: 1.46
• Siedepunkt (°C): 65°C/2.3mmHg(lit.)
• Molekulargewicht: 227.100 g/mol
• XLogP3: 0.400
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 8
• Exact Mass: 226.02 Da
• Monoisotopic Mass: 226.02 Da
• Topological Polar Surface Area: 27.700 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 70.700
• 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

Referenzen

1. 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]