2-Chloroethyl methyl ether, 98%
2-Chloroethyl methyl ether, 98%
2-Chloroethyl methyl ether, 98%
Thermo Scientific Chemicals

2-Chloroethyl methyl ether, 98%

CAS: 627-42-9 | C3H7ClO | 94.54 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
25 g
100 g
500 g
Catalog number B24081.22
also known as B24081-22
Price (USD)
112.65
Online Exclusive
125.00
Save 12.35 (10%)
Each
Quantity:
100 g
Request bulk or custom format
Price (USD)
112.65
Online Exclusive
125.00
Save 12.35 (10%)
Each
Chemical Identifiers
CAS627-42-9
IUPAC Name1-chloro-2-methoxyethane
Molecular FormulaC3H7ClO
InChI KeyXTIGGAHUZJWQMD-UHFFFAOYSA-N
SMILESCOCCCl
View more
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear, colorless to yellow
Assay (GC)>97.5%
FormLiquid
Refractive Index1.4070-1.4110 @ 20?C
2-Chloroethyl methyl ether was used in the synthesis of acyclic nucleosides of thieno[2,3-d] pyrimidine derivatives.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2-Chloroethyl methyl ether was used in the synthesis of acyclic nucleosides of thieno[2,3-d] pyrimidine derivatives.

Solubility
Soluble in water 60 g/L at 20°C.

Notes
Store away from oxidizing agents, bases.
RUO – Research Use Only

General References:

  1. Nasser A Hassan; Mohamed I Hegab; Aymn E Rashad; Afaf A Fahmy;Synthesis and antimicrobial activity of some cyclic and acyclic nucleosides of thieno[2,3-d]pyrimidines. Nucleosides, Nucleotides & Nucleic Acids. 2007, 26 (4), 379-390.
  2. E. A. C. Lucken. Chemical applications of nuclear quadrupole resonance spectroscopy. Part III. The inductive effect of substituents belonging to the first row of the periodic table. J. Chem. Soc. 1959, 2954-2960.