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

CAS: 6482-24-2 Cat. No.: B139139 Molecular Weight: 138.99 Beilstein Registry Number: 1(1)171 EC Number: 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

Overview

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

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

Specifications & Purity

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

Storage

Store at 2-8°C, Argon charged

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥95%(GC)

Names and Identifiers

• Pubchem Sid: 504755488
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504755488
• Canonical Smiles: COCCBr
• IUPAC Name: 1-bromo-2-methoxyethane
• InChIKey: YZUPZGFPHUVJKC-UHFFFAOYSA-N
• INCHI: 1S/C3H7BrO/c1-5-3-2-4/h2-3H2,1H3
• Isomeric SMILES: COCCBr
• WGK Germany: 3
• Molecular Weight: 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
    • Class Organooxygen compounds
      • Subclass Ethers

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: 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

Chemical and Physical Properties

• Solubility: Soluble in water.14,4 g/L at 25°C
• Sensitivity: air & heat sensitive
• Refractive Index: 1.448
• Flash Point(°F): 82.4 °F
• Flash Point(°C): 28 °C
• Boil Point(°C): 40-41 °C/66 mmHg
• Molecular Weight: 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

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