2-Methoxyethyl chloroformate

Synonym: 2-methoxyethyl chlorocarbonate; 2-Methoxyethyl carbonochloridate; (2-Methoxyethoxy)carbonyl chloride; (Chloro)(2-methoxyethoxy)methanone; Chloroformic acid 2-methoxyethyl ester
Molecular Formula: CH3OCH2CH2OCOCl
Molecular Weight: 138.55
CAS Number: 628-12-6
MDL number: MFCD00058932
EC Number: 211-026-9
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Packing size: 5 ML  
34.30 EUR
Packing size: 25 ML  
86.10 EUR



Safety Information


Hazard Statements

H314
H226
H330

Precautionary Statements

P210
P280
P303 + P361 + P353
P264
P501
P305 + P351 + P338
P271
P233
P240
P241
P242
P405
P403 + P235
P260
P243
P403 + P233
P284
P370 + P378
P301 + P330 + P331
P363
P304 + P340
P321
P316

Pictograms

 Product Description

2-Methoxyethyl chloroformate is an organic compound with a chloroformate functional group attached to a 2-methoxyethyl chain. It is used as a reagent in organic synthesis and chemical modification processes.

 

Application

This compound is utilized in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, serving as a protecting group reagent and intermediate in various chemical reactions.

 

 

Articles:

- DMEAD: a new dialkyl azodicarboxylate for the Mitsunobu reaction

Publication Date: Available online 27 May 2009

Kazutake Hagiya, Natsuko Muramoto, Tomonori Misaki, Takashi Sugimura

https://doi.org/10.1016/j.tet.2009.05.048

 

- Development of hedgehog pathway inhibitors by epigenetically targeting GLI through BET bromodomain for the treatment of medulloblastoma

Publication Date: Available online 21 July 2020

Xiaohua Liu, Yu Zhang, Yalei Li, Juan Wang, Huaqian Ding, Wenjing Huang, Chunyong Ding, Hongchun Liu, Wenfu Tan, Ao Zhang

https://doi.org/10.1016/j.apsb.2020.07.007

 

- Green Chemistry Articles of Interest to the Pharmaceutical Industry

Publication Date: September 19, 2008

Stephen Challenger, Leo Dudin, Jimmy DaSilva, Peter Dunn, Tom Govaerts, John Hayler, Bill Hinkley, Yannis Houpis, Thomas Hunter, Lisa Jellet, John L. Leazer, Jr., Kurt Lorenz, Suju Mathew, Thomas Rammeloo, Ravinder Sudini, Zonghui Wan, Chris Welch, Andrew Wells, Jennifer Vance, Chaoyu Xie and Fuyao Zhang

https://doi.org/10.1021/op800175p