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5187-23-5

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5187-23-5 Usage

General Description

Physical properties (such as boiling point, refractive index and density) of 5-ethyl-1,3-dioxane-5-methanol have been reported.

Check Digit Verification of cas no

The CAS Registry Mumber 5187-23-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,8 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5187-23:
(6*5)+(5*1)+(4*8)+(3*7)+(2*2)+(1*3)=95
95 % 10 = 5
So 5187-23-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O3/c1-2-7(3-8)4-9-6-10-5-7/h8H,2-6H2,1H3

5187-23-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Ethyl-1,3-dioxane-5-methanol

1.2 Other means of identification

Product number -
Other names (5-Ethyl-1,3-dioxan-5-yl)methanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5187-23-5 SDS

5187-23-5Synthetic route

formaldehyd
50-00-0

formaldehyd

1,1,1-tri(hydroxymethyl)propane
77-99-6

1,1,1-tri(hydroxymethyl)propane

5-ethyl-1,3-dioxane-5-methanol
5187-23-5

5-ethyl-1,3-dioxane-5-methanol

Conditions
ConditionsYield
With cationite KU-2 In benzene Reflux; Dean-Stark;97%
With toluene-4-sulfonic acid In toluene for 4h; Heating;95%
With toluene-4-sulfonic acid In toluene for 4h; Heating;95%
With toluene-4-sulfonic acid In tetrahydrofuran for 3h; Reflux;93%
With toluene-4-sulfonic acid
Dimethoxymethane
109-87-5

Dimethoxymethane

1,1,1-tri(hydroxymethyl)propane
77-99-6

1,1,1-tri(hydroxymethyl)propane

5-ethyl-1,3-dioxane-5-methanol
5187-23-5

5-ethyl-1,3-dioxane-5-methanol

Conditions
ConditionsYield
With toluene-4-sulfonic acid; lithium bromide In dichloromethane at 20℃; for 0.416667h;88%
Reaxys ID: 11464418

Reaxys ID: 11464418

A

1,1,1-tri(hydroxymethyl)propane
77-99-6

1,1,1-tri(hydroxymethyl)propane

B

3,3,7,7-tetra(hydroxymethyl)-5-oxanonane
23235-61-2

3,3,7,7-tetra(hydroxymethyl)-5-oxanonane

C

5-ethyl-1,3-dioxane-5-methanol
5187-23-5

5-ethyl-1,3-dioxane-5-methanol

Conditions
ConditionsYield
With toluene-4-sulfonic acid In water at 90℃; for 6h;A n/a
B 5.9 g
C n/a
With toluene-4-sulfonic acid In water at 90℃; for 6h;A n/a
B 15.2 g
C n/a
5-ethyl-1,3-dioxane-5-methanol
5187-23-5

5-ethyl-1,3-dioxane-5-methanol

acrylic acid methyl ester
292638-85-8

acrylic acid methyl ester

5-acryloxymethyl-5-ethyl-1,3-dioxacyclohexane

5-acryloxymethyl-5-ethyl-1,3-dioxacyclohexane

Conditions
ConditionsYield
With dioctyltin(IV) oxide; 4-methoxy-phenol In hexane at 75 - 90℃;94.1%
With dioctyltin(IV) oxide; 4-methoxy-phenol In hexane at 75 - 90℃; under 760.051 Torr; for 25h;88%
5-ethyl-1,3-dioxane-5-methanol
5187-23-5

5-ethyl-1,3-dioxane-5-methanol

acetyl chloride
75-36-5

acetyl chloride

Acetic acid 5-ethyl-[1,3]dioxan-5-ylmethyl ester

Acetic acid 5-ethyl-[1,3]dioxan-5-ylmethyl ester

Conditions
ConditionsYield
With triethylamine In chloroform90%
5-ethyl-1,3-dioxane-5-methanol
5187-23-5

5-ethyl-1,3-dioxane-5-methanol

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

methyl (5-ethyl-1,3-dioxan-5-yl)methyl carbonate

methyl (5-ethyl-1,3-dioxan-5-yl)methyl carbonate

Conditions
ConditionsYield
With dimanganese decacarbonyl at 180℃; for 1h; Autoclave;84%
5-ethyl-1,3-dioxane-5-methanol
5187-23-5

5-ethyl-1,3-dioxane-5-methanol

acetylene
74-86-2

acetylene

5-ethyl-5-vinyloxymethyl-1,3-dioxane
1159490-98-8

5-ethyl-5-vinyloxymethyl-1,3-dioxane

Conditions
ConditionsYield
With potassium hydroxide at 110 - 125℃; under 9120.61 Torr; for 2h;80%
5-ethyl-1,3-dioxane-5-methanol
5187-23-5

5-ethyl-1,3-dioxane-5-methanol

acrylic acid
79-10-7

acrylic acid

5-acryloxymethyl-5-ethyl-1,3-dioxacyclohexane

5-acryloxymethyl-5-ethyl-1,3-dioxacyclohexane

Conditions
ConditionsYield
With methanesulfonic acid; hydroquinone In hexane at 90℃; under 760.051 Torr; for 15h;60%
bis(diethylamino)dimethylsilane
4669-59-4

bis(diethylamino)dimethylsilane

5-ethyl-1,3-dioxane-5-methanol
5187-23-5

5-ethyl-1,3-dioxane-5-methanol

dimethyl(5-ethyl-1,3-dioxacyclohexyl)-5-methoxysilane

dimethyl(5-ethyl-1,3-dioxacyclohexyl)-5-methoxysilane

Conditions
ConditionsYield
In 1,4-dioxane Heating;48%
5-ethyl-1,3-dioxane-5-methanol
5187-23-5

5-ethyl-1,3-dioxane-5-methanol

acryloyl chloride
814-68-6

acryloyl chloride

5-acryloxymethyl-5-ethyl-1,3-dioxacyclohexane

5-acryloxymethyl-5-ethyl-1,3-dioxacyclohexane

Conditions
ConditionsYield
With triethylamine In chloroform for 0.5h;
With triethylamine In chloroform
oxirane
75-21-8

oxirane

monomethylmonoformal

monomethylmonoformal

monomethyldiformal

monomethyldiformal

bis-TMP

bis-TMP

5-ethyl-1,3-dioxane-5-methanol
5187-23-5

5-ethyl-1,3-dioxane-5-methanol

polyetherol

polyetherol

Conditions
ConditionsYield
Stage #1: monomethylmonoformal; monomethyldiformal; bis-TMP; 5-ethyl-1,3-dioxane-5-methanol With potassium hydroxide In water at 100 - 120℃; under 15.0015 Torr;
Stage #2: oxirane at 90 - 160℃; for 1h;
Stage #3: With phosphoric acid; water Product distribution / selectivity; more than 3 stages;
ethyl 2-diazo-3-oxobutanoate
2009-97-4

ethyl 2-diazo-3-oxobutanoate

5-ethyl-1,3-dioxane-5-methanol
5187-23-5

5-ethyl-1,3-dioxane-5-methanol

A

ethyl (Z)-8-ethyl-8-(hydroxymethyl)-4-methyl-1,3,6-trioxacyclonon-4-ene-5-carboxylate

ethyl (Z)-8-ethyl-8-(hydroxymethyl)-4-methyl-1,3,6-trioxacyclonon-4-ene-5-carboxylate

B

ethyl (Z)-8-ethyl-8-(hydroxymethyl)-5-methyl-1,3,6-trioxacyclonan-4-ene-4-carboxylate

ethyl (Z)-8-ethyl-8-(hydroxymethyl)-5-methyl-1,3,6-trioxacyclonan-4-ene-4-carboxylate

Conditions
ConditionsYield
With copper(II) bis(trifluoromethanesulfonate) In benzene at 80℃; for 6h; Overall yield = 40 %;
poly(methacrylic acid)
79-41-4

poly(methacrylic acid)

5-ethyl-1,3-dioxane-5-methanol
5187-23-5

5-ethyl-1,3-dioxane-5-methanol

(5-ethyl-1,3-dioxan-5-yl)methyl-2-methyl acrylate

(5-ethyl-1,3-dioxan-5-yl)methyl-2-methyl acrylate

Conditions
ConditionsYield
With toluene-4-sulfonic acid
5-ethyl-1,3-dioxane-5-methanol
5187-23-5

5-ethyl-1,3-dioxane-5-methanol

maleic acid
110-16-7

maleic acid

1,4-bis(5-ethyl-1,3-dioxan-5-yl)methyl maleate

1,4-bis(5-ethyl-1,3-dioxan-5-yl)methyl maleate

Conditions
ConditionsYield
With toluene-4-sulfonic acid

5187-23-5Downstream Products

5187-23-5Relevant articles and documents

Contributions from interfacial polarization, conductivity and polymer relaxations to the complex permittivity of a film of poly[(5-ethyl-1,3-dioxan-5-yl)methyl acrylate] containing ionic impurities

Sorensen, Torben Smith,Diaz-Calleja, Ricardo,Riande, Evaristo,Guzman, Julio,Andrio, Andreu

, p. 2399 - 2411 (1997)

The complex permittivity of a film of the polymer poly[(5-ethyl-1,3-dioxan-5-yl)methyl acrylate] of width 0.4 mm and containing very small amounts of ionic impurities has been studied at a range of frequencies from 0.01 Hz to 100 kHz and at a range of temperatures from -135 to +140°C. Some mechanical determinations of the complex Young modulus have also been performed for the same polymer. To separate the surface polarisation effects and the conductivity effects from the dielectric relaxations of the polymer chains and side-chains we have used the same theoretical methods as earlier described for a film of a copolymer of vinylidene cyanide and vinyl acetate and for a film of poly[4-(acryloxy)phenyl-(4-chlorophenyl)methanone]. The diffusion coefficient of the most rapidly diffusing ion is studied as a function of temperature. The diffusion coefficient follows a non-Arrhenius Vogel relation with the same Vogel temperature as the α-relaxation (glass-rubber). Both phenomena may be interpreted using the Cohen-Turnbull theory of free volume as has previously been done for the diffusion of oxygen through poly(cyclohexyl acrylate). The fractional free volume at the glass transition temperature (ca. 36°C) is found to be 0.031, close to the range normally found (0.025 ± 0.005). A β-relaxation is also found at higher frequencies and lower temperatures. This relaxation shows Arrhenius behaviour with an activation energy E?/R = 5780 K. The α- and β-relaxations seem to merge at ca. 100°C and in addition a relaxation more slow than the α-relaxation is found at even higher temperatures. This relaxation can only be seen after correction of the dielectric loss for conductivity. The mean activation energy of this relaxation in the temperature range 90-140°C is practically identical with the mean activation energy of the α-relaxation in the same range of temperatures (E?/R ≈ 15 000 K). The slow relaxation is probably connected with the motion of the polymer molecule as a whole in the 'virtual tubes' of long-range, topological entanglements, for example by 'reptation'. At very high frequencies (50-100 kHz), isochronous graphs of dielectric loss vs. temperature exhibit a splitting of the α-peak into two peaks.

Synthesis and bactericidal activity of substituted cyclic acetals

Tugarova,Kazakova,Kamnev,Zlotskii

, p. 1930 - 1933 (2015/02/02)

A series of substituted cyclic acetals were synthesized and tested for their bactericidal activity against bacteria strain Azospirillum brasilense Sp245.

Process for recovering ditrimethylolpropane

-

Example 4, (2008/06/13)

The present invention provides processes for recovering ditrimethylolpropane from a still residue obtained by extracting and then distilling off trimethylolpropane from a reaction solution obtained by reacting n-butyraldehyde with formaldehyde in the presence of a basic catalyst.One process comprises acid decomposition of formals in the still residue.A second process comprises removal from the still residue of components having a higher boiling point than that of ditrimethylolpropane followed by crystallization of the resultant product.

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