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ChemicalBook--->CAS DataBase List--->6136-93-2

6136-93-2

6136-93-2 Structure

6136-93-2 Structure
IdentificationBack Directory
[Name]

DIETHOXYACETONITRILE
[CAS]

6136-93-2
[Synonyms]

Einecs 228-111-1
DIETHOXYACETONITRILE
diethoxy-acetonitril
Acetonitrile, diethoxy-
2,2-diethoxyacetonitrile
1,1-Diethoxyacetonitrile
Acetonitrile, 2,2-diethoxy-
2,2-Diethoxyacetonitrile,98%
DIETHOXYACETONITRILE ISO 9001:2015 REACH
[EINECS(EC#)]

228-111-1
[Molecular Formula]

C6H11NO2
[MDL Number]

MFCD00043982
[MOL File]

6136-93-2.mol
[Molecular Weight]

129.16
Chemical PropertiesBack Directory
[Melting point ]

−19-−18 °C(lit.)
[Boiling point ]

167.7 °C773 mm Hg(lit.)
[density ]

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

n20/D 1.4(lit.)
[Fp ]

121 °F
[storage temp. ]

Inert atmosphere,2-8°C
[InChIKey]

UDELMRIGXNCYLU-UHFFFAOYSA-N
[EPA Substance Registry System]

Acetonitrile, diethoxy- (6136-93-2)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

10-20/21/22-36/37/38
[Safety Statements ]

16-26-27-36/37/39
[RIDADR ]

UN 1993 3/PG 3
[WGK Germany ]

3
[HazardClass ]

3.2
[PackingGroup ]

III
Hazard InformationBack Directory
[Uses]

Diethoxyacetonitrile may be used in the preparation of methyl 5-diethoxymethylimidazole-4-carboxylate, via anionic cycloaddition reaction with methyl isocyanoacetate.
[General Description]

Diethoxyacetonitrile is a 2,2-dialkoxyalkanenitrile derivative. Reaction of hydrocyanic acid with various ortho esters of aliphatic and aromatic acids in the presence of acidic catalyst has been reported to afford diethoxyacetonitrile. Houben-Hoesch reaction of diethoxyacetonitrile with 1,2,4-trimethoxybenzene affords tris(2,4,5-trimethoxyphenyl)methane.
Spectrum DetailBack Directory
[Spectrum Detail]

DIETHOXYACETONITRILE(6136-93-2)1HNMR
DIETHOXYACETONITRILE(6136-93-2)IR
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