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53185-52-7

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53185-52-7 Usage

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 53185-52-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,1,8 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53185-52:
(7*5)+(6*3)+(5*1)+(4*8)+(3*5)+(2*5)+(1*2)=117
117 % 10 = 7
So 53185-52-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO2/c1-7(2)6(8)4-5-9-3/h4-5H2,1-3H3

53185-52-7SDS

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 3-methoxy-N,N-dimethylpropanamide

1.2 Other means of identification

Product number -
Other names EINECS 258-420-7

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:53185-52-7 SDS

53185-52-7Synthetic route

methyl 3-methoxypropionate
3852-09-3

methyl 3-methoxypropionate

dimethyl amine
124-40-3

dimethyl amine

β-methoxy-N,N-dimethylpropionic acid amide
53185-52-7

β-methoxy-N,N-dimethylpropionic acid amide

Conditions
ConditionsYield
With zinc(II) trifluoroacetate at 0 - 40℃; for 8h; Reagent/catalyst; Autoclave;99%
With sodium methylate; glycerol at 60℃; for 6h; Autoclave;86%
With potassium tert-butylate at 20℃; under 600.06 Torr; for 4h; Product distribution / selectivity; Autoclave;
With sodium methylate; ethylene glycol at 60℃; for 8h; Product distribution / selectivity; Autoclave;
C6H12O4

C6H12O4

C10H18O6

C10H18O6

dimethyl amine
124-40-3

dimethyl amine

β-methoxy-N,N-dimethylpropionic acid amide
53185-52-7

β-methoxy-N,N-dimethylpropionic acid amide

Conditions
ConditionsYield
at 60℃; for 6h; Autoclave;
methanol
67-56-1

methanol

N,N-Dimethylacrylamide
2680-03-7

N,N-Dimethylacrylamide

β-methoxy-N,N-dimethylpropionic acid amide
53185-52-7

β-methoxy-N,N-dimethylpropionic acid amide

Conditions
ConditionsYield
With sodium methylate at 20 - 40℃; Product distribution / selectivity; Inert atmosphere;
With 2-Cyanopyridine; cerium(IV) oxide at 49.84℃; for 24h; Kinetics;
3-(N,N-dimethylamino)-N',N'-dimethylpropionamide
17268-47-2

3-(N,N-dimethylamino)-N',N'-dimethylpropionamide

β-methoxy-N,N-dimethylpropionic acid amide
53185-52-7

β-methoxy-N,N-dimethylpropionic acid amide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: hydroquinone; cupferron / alumina N611N / water / 5 h / 250 °C / 2250.23 Torr
2: sodium methylate / 20 - 40 °C / Inert atmosphere
View Scheme
3-Methoxypropionic acid
2544-06-1

3-Methoxypropionic acid

dimethyl amine
124-40-3

dimethyl amine

β-methoxy-N,N-dimethylpropionic acid amide
53185-52-7

β-methoxy-N,N-dimethylpropionic acid amide

Conditions
ConditionsYield
at 100℃; under 11251.1 Torr; Temperature; Pressure;
at 100℃; under 11251.1 Torr; Temperature; Pressure; Concentration;
β-methoxy-N,N-dimethylpropionic acid amide
53185-52-7

β-methoxy-N,N-dimethylpropionic acid amide

N,N-Dimethylacrylamide
2680-03-7

N,N-Dimethylacrylamide

Conditions
ConditionsYield
With 4-methoxy-phenol; potassium hydroxide In ethylene glycol at 200℃; Temperature; Reagent/catalyst; Pyrolysis;98%
With 10H-phenothiazine; copper(II) bis(trifluoromethanesulfonate) at 130℃; for 6h; Inert atmosphere;92%
β-methoxy-N,N-dimethylpropionic acid amide
53185-52-7

β-methoxy-N,N-dimethylpropionic acid amide

4-chlorobenzoic acid hydrazide
536-40-3

4-chlorobenzoic acid hydrazide

C11H11ClN2O2

C11H11ClN2O2

Conditions
ConditionsYield
With titanium tetrachloride at 110℃; for 1.5h;74%

53185-52-7Downstream Products

53185-52-7Relevant articles and documents

Synthesis method of 3-methoxyl-N, N-dimethylacrylamide

-

Paragraph 0041-0044, (2017/07/22)

The invention relates to a synthesis method of 3-methoxyl-N, N-dimethylacrylamide, and belongs to the technical field of chemical synthesis. The synthesis method comprises the following steps of adding 3-methoxypropionic acid and dimethylamine into a sealed reactor; raising the temperature to 80 to 150 DEG C; performing reaction to obtain 3-methoxyl-N, N-dimethylacrylamide, wherein the pressure in the sealed reactor is 0.1 to 10.0MPa. The 3-methoxypropionic acid is used as the raw materials to perform high-temperature dewatering with dimethylamine in a sealed reaction vessel; polyhydric alcohol and basic catalysts are not needed; the reaction is simple; the implementation is easy; the yield of a product is high; the purity is high; the high yield is realized; meanwhile, the pollution is little; the cost is low; the method conforms to the requirements of modern chemical green synthesis. Meanwhile, the 3-methoxypropionic acid uses low-price acrylonitrile as the starting raw materials; the acrylonitrile is subjected to alkoxylation to obtain methoxyl propionitrile; then, hydrolysis is performed. The operation is simple; the energy consumption is low.

Formation of a New, Strongly Basic Nitrogen Anion by Metal Oxide Modification

Tamura, Masazumi,Kishi, Ryota,Nakayama, Akira,Nakagawa, Yoshinao,Hasegawa, Jun-Ya,Tomishige, Keiichi

supporting information, p. 11857 - 11867 (2017/09/08)

Development of new hybrid materials having unique and unprecedented catalytic properties is a challenge for chemists, and heterogeneous-homogeneous hybrid catalysts have attracted much attention because of the preferable and exceptional properties that are highly expected to result from combination of the components. Base catalysts are widely used in organic synthesis as key materials, and a new class of base catalysts has made a large impact from academic and industrial viewpoints. Here, a principle for creating a new strong base by hybridization of homogeneous and heterogeneous components is presented. It is based on the modification of organic compounds with metal oxides by using the acid-base property of metal oxides. Based on kinetic and DFT studies, combination of CeO2 and 2-cyanopyridine drastically enhanced the basicity of 2-cyanopyridine by a factor of about 109 (~9 by pKa (in CH3CN)), and the pKa was estimated to be ~21, which locates it in the superbase category. 2-Cyanopyridine and CeO2 formed a unique adsorption complex via two interaction modes: (i) coordinative interaction between the Ce atom of CeO2 and the N atom of the pyridine ring in 2-cyanopyridine, and (ii) covalent interaction between the surface O atom of CeO2 and the C atom of the CN group in 2-cyanopyridine by addition of the lattice oxygen of CeO2 to the CN group of 2-cyanopyridine. These interactions established a new, strongly basic site of N- over the CeO2 surface.

METHOD FOR PRODUCING BETA -ALKOXYPROPIONAMIDE

-

Paragraph 0060; 0061; 0062; 0063; 0064, (2015/03/03)

A method for producing a β-alkoxypropionamide including reacting a β-alkoxypropionic acid ester represented by the following formula (1) and an amine represented by the following formula (2) in the presence of a polyol and a basic catalyst, thereby to produce a β-alkoxypropionamide represented by the following formula (3), wherein, as the polyol, a reaction residue that is generated by the reaction and contains a used polyol is used: (wherein in the formulas, R and R' are independently a C1 to C6 linear, branched or cyclic, saturated hydrocarbon group; R1 and R2 are independently a C1 to C6 linear, branched or cyclic, saturated hydrocarbon group; and R3 is H or CH3).

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