ChemicalBook > Product Catalog > Chemical Reagents > Organic reagents > Esters > Ethyl compound > 2-METHOXYETHYL CHLOROFORMATE
2-METHOXYETHYL CHLOROFORMATE
2-METHOXYETHYL CHLOROFORMATE Basic information
- Product Name:
- 2-METHOXYETHYL CHLOROFORMATE
- Synonyms:
-
- 2-Methoxyethyl chloroformate, tech. 85%
- (2-Methoxyethoxy)carbonyl chloride
- (Chloro)(2-methoxyethoxy)methanone
- 2-methoxyethyl carbonochloridate
- chlorocarbonic acid 2-methoxyethyl ester
- Chloroformic Acid 2-Methoxyethyl Ester Ethylene Glycol Monomethyl Ether Chloroformate
- CHLOROFORMIC ACID 2-METHOXYETHYL ESTER
- ETHYLENE GLYCOL MONOMETHYL ETHER CHLOROFORMATE
- CAS:
- 628-12-6
- MF:
- C4H7ClO3
- MW:
- 138.55
- EINECS:
- 211-026-9
- Product Categories:
-
- Acid Halides
- Building Blocks
- Acid Halides
- Carbonyl Compounds
- Chemical Synthesis
- Organic Building Blocks
- CHLOROFORMATES
- Carbonyl Compounds
- Organic Building Blocks
- Mol File:
- 628-12-6.mol
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2-METHOXYETHYL CHLOROFORMATE Chemical Properties
- Boiling point:
- 157-158 °C(lit.)
- Density
- 1.192 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.4200(lit.)
- Flash point:
- 138 °F
- storage temp.
- 2-8°C
- solubility
- Soluble in most organic solvents.
- form
- clear liquid
- color
- Colorless to Light yellow
- Sensitive
- Moisture Sensitive
- CAS DataBase Reference
- 628-12-6(CAS DataBase Reference)
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Safety Information
- Hazard Codes
- C
- Risk Statements
- 34
- Safety Statements
- 26-36/37/39-45
- RIDADR
- UN 2920 8/PG 2
- WGK Germany
- 3
- F
- 10-21
- HS Code
- 2918.99.5000
- HazardClass
- 6.1
- PackingGroup
- II
MSDS
- Language:English Provider:SigmaAldrich
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2-METHOXYETHYL CHLOROFORMATE Usage And Synthesis
Uses
Reactant for:• ;Preparation of N-bridged bicyclic sulfonamides as inhibitors of γ-secretase1• ;Preparation of dimethoxyethyl azodicarboxylate via amidation/oxidation and application to Mitsunobu reaction2• ;Regioselective, stereoselective, and kinetically-controlled nickel-catalyzed cyanoesterification of allenes chloroformates and TMSCN3• ;Preparation of amino carboxamidobenzothiazoles as Lck inhibitors4• ;Preparation of nonracemic spirooxindoles using a stereoselective three-component coupling reaction as the key step and using acylation reactions to add st
Uses
2-methoxyethyl chloroformate was used to produce di-2-dimethoxyethyl hydrazine carboxylate(alternative reagent for the mitsunobu reaction).
2-METHOXYETHYL CHLOROFORMATESupplier
J & K SCIENTIFIC LTD.
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- 010-82848833 400-666-7788
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- Tel
- 400-6106006
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- 021-67121386
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Energy Chemical
- Tel
- 021-021-58432009 400-005-6266
- sales8178@energy-chemical.com
Wuhan Chemwish Technology Co., Ltd
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- 86-027-67849912
- sales@chemwish.com
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2-METHOXYETHYL CHLOROFORMATE(628-12-6)Related Product Information
- Ethyl formate
- 1-Methyl-2-methoxyethyl chloroformate
- 2-Ethoxyethyl chloroformate
- 2-BENZYLOXYETHYL CHLOROFORMATE
- 2-Phenoxyethyl chloroformate
- ETHYLENEBIS(CHLOROFORMATE)
- TRIETHYLENE GLYCOL BIS(CHLOROFORMATE)
- 3,6-BIS[(CHLOROCARBONYL)OXY]HEXAHYDROFURO[3,2-B]FURAN
- Oxydiethylene bis(chloroformate)
- 2-METHOXYETHYL CHLOROFORMATE