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CAS No.: | 13352-76-6 |
---|---|
Name: | 2,4,6,8,10,12-Hexaoxatridecane |
Article Data: | 9 |
Molecular Structure: | |
Formula: | C7H16O6 |
Molecular Weight: | 196.2 |
Synonyms: | 1,9-dimethoxy-2,4,6,8-tetraoxa-nonane;CH3-(OCH2)5-OCH3;bis-(methoxymethoxy-methoxy)-methane;2,4,6,8,10,12-Hexaoxatridecane; |
Density: | 1.1003 g/cm3(Temp: 25 °C) |
Melting Point: | 18.3 °C |
Boiling Point: | 123-135℃/8Torr |
PSA: | 55.38000 |
LogP: | 0.13310 |
1,3,5-Trioxan
1,1-dimethoxyethane
C
bis-methoxymethoxy-methane
D
bis(methoxymethyl)ether
E
POMM4
F
CH3-(OCH2)8-OCH3
G
Methoxymethoxymethoxymethoxymethoxy-methoxymethoxymethoxymethoxymethoxymethoxy-methane
H
POMM5
I
CH3-(OCH2)7-OCH3
J
CH3-(OCH2)6-OCH3
Conditions | Yield |
---|---|
Amberlite IR 120 at 100℃; for 24h; Product distribution / selectivity; | |
trifluorormethanesulfonic acid at 100℃; for 40h; Product distribution / selectivity; | |
sulfuric acid In water at 100℃; for 12h; Product distribution / selectivity; |
1,3,5-Trioxan
1,1-dimethoxyethane
bis(methoxymethyl)ether
C
bis-methoxymethoxy-methane
D
POMM4
E
CH3-(OCH2)8-OCH3
F
Methoxymethoxymethoxymethoxymethoxy-methoxymethoxymethoxymethoxymethoxymethoxy-methane
G
POMM5
H
CH3-(OCH2)7-OCH3
I
CH3-(OCH2)6-OCH3
Conditions | Yield |
---|---|
sulfuric acid In water at 100℃; for 12h; Product distribution / selectivity; |
1,3,5-Trioxan
bis(methoxymethyl)ether
C
1,1-dimethoxyethane
D
bis-methoxymethoxy-methane
E
POMM4
F
CH3-(OCH2)8-OCH3
G
Methoxymethoxymethoxymethoxymethoxy-methoxymethoxymethoxymethoxymethoxymethoxy-methane
H
POMM5
I
CH3-(OCH2)7-OCH3
J
CH3-(OCH2)6-OCH3
Conditions | Yield |
---|---|
sulfuric acid In water at 100℃; for 12h; Product distribution / selectivity; |
formaldehyd
1,1-dimethoxyethane
C
bis-methoxymethoxy-methane
D
bis(methoxymethyl)ether
E
POMM4
F
CH3-(OCH2)8-OCH3
G
Methoxymethoxymethoxymethoxymethoxy-methoxymethoxymethoxymethoxymethoxymethoxy-methane
H
POMM5
I
CH3-(OCH2)7-OCH3
J
CH3-(OCH2)6-OCH3
Conditions | Yield |
---|---|
Amberlite IR 120 at 100℃; for 8h; Product distribution / selectivity; |
methanol
formaldehyd
A
bis-methoxymethoxy-methane
B
POMM4
C
POMM5
Conditions | Yield |
---|---|
With C16H36NO3S(1+)*CH3O4S(1-) at 125 - 130℃; under 26252.6 - 30003 Torr; Reagent/catalyst; Inert atmosphere; |
methanol
formaldehyd
A
Dimethoxymethane
B
bis-methoxymethoxy-methane
C
bis(methoxymethyl)ether
D
POMM4
E
POMM5
Conditions | Yield |
---|---|
With C16H36NO3S(1+)*CH3O4S(1-) In water at 125 - 130℃; under 26252.6 - 30003 Torr; Reagent/catalyst; |
Conditions | Yield |
---|---|
With C13H25N2O3S(1+)*HO4S(1-) at 150℃; for 10h; Autoclave; |
1,3,5-Trioxan
Dimethoxymethane
A
bis-methoxymethoxy-methane
B
bis(methoxymethyl)ether
C
POMM4
D
POMM5
Conditions | Yield |
---|---|
With C10-AS-50 at 105℃; under 9750.98 Torr; for 2h; Catalytic behavior; Inert atmosphere; |
formaldehyd
Dimethoxymethane
A
bis-methoxymethoxy-methane
B
bis(methoxymethyl)ether
C
POMM4
D
CH3-(OCH2)8-OCH3
E
POMM5
F
CH3-(OCH2)7-OCH3
G
CH3-(OCH2)6-OCH3
Conditions | Yield |
---|---|
With lanthanum(III) sulfate at 130℃; under 3750.38 Torr; for 6h; Reagent/catalyst; Concentration; Time; Temperature; Pressure; Overall yield = 75.5 %; | A 20.74 %Chromat. B 25.87 %Chromat. C 13.77 %Chromat. D 1.11 %Chromat. E 8.14 %Chromat. F 2.37 %Chromat. G 4.23 %Chromat. |
formaldehyd
Dimethoxymethane
A
Dimethyl ether
B
Methyl formate
C
POMM5
Conditions | Yield |
---|---|
With C16AlF36O4(1-)*C3H9O(1+) at 25 - 30℃; Schlenk technique; Inert atmosphere; |