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ChemicalBook--->CAS DataBase List--->628-12-6

628-12-6

628-12-6 Structure

628-12-6 Structure
IdentificationMore
[Name]

2-METHOXYETHYL CHLOROFORMATE
[CAS]

628-12-6
[Synonyms]

2-METHOXYETHYL CHLOROFORMATE
CHLOROFORMIC ACID 2-METHOXYETHYL ESTER
ETHYLENE GLYCOL MONOMETHYL ETHER CHLOROFORMATE
2-Methoxyethyl chloroformate, tech. 85%
[EINECS(EC#)]

211-026-9
[Molecular Formula]

C4H7ClO3
[MDL Number]

MFCD00058932
[Molecular Weight]

138.55
[MOL File]

628-12-6.mol
Chemical PropertiesBack Directory
[Boiling point ]

157-158 °C(lit.)
[density ]

1.192 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.4200(lit.)
[Fp ]

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)
Safety DataBack Directory
[Hazard Codes ]

C
[Risk Statements ]

R34:Causes burns.
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
[RIDADR ]

UN 2920 8/PG 2
[WGK Germany ]

3
[F ]

10-21
[HS Code ]

2918.99.5000
[HazardClass ]

6.1
[PackingGroup ]

II
Hazard InformationBack Directory
[Uses]

2-methoxyethyl chloroformate was used to produce di-2-dimethoxyethyl hydrazine carboxylate(alternative reagent for the mitsunobu reaction).
[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
Spectrum DetailBack Directory
[Spectrum Detail]

2-METHOXYETHYL CHLOROFORMATE(628-12-6)MS
2-METHOXYETHYL CHLOROFORMATE(628-12-6)1HNMR
2-METHOXYETHYL CHLOROFORMATE(628-12-6)13CNMR
2-METHOXYETHYL CHLOROFORMATE(628-12-6)IR1
2-METHOXYETHYL CHLOROFORMATE(628-12-6)Raman
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

2-Methoxyethyl chloroformate, tech. 85%(628-12-6)
[Sigma Aldrich]

628-12-6(sigmaaldrich)
[TCI AMERICA]

2-Methoxyethyl Chloroformate,>80.0%(GC)(T)(628-12-6)
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