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

CAS: 72593-77-2 Cat. No.: B471551 Formule: C₇H₁₅BrO₃ Poids moléculaire: 227.1 Numéro CE: 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

Synonymes

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

Spécifications et pureté

≥97%

Conditions de stockage de stockage

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

Expédié en

Wet ice

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Pureté

≥97%

Noms et identifiants

• Pubchem Sid: 488198380
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488198380
• Sourires canoniques: 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
• Isomères SMILES: COCCOCCOCCBr
• Poids moléculaire: 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
    • 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
• Description: 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

Propriétés chimiques et physiques

• Sensibilité: moisture sensitive；heat sensitive；air sensitive；light sensitive
• Indice de réfraction: 1.46
• Point d'ébullition (°C): 65°C/2.3mmHg(lit.)
• Poids moléculaire: 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

Références

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]