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1117-37-9

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1117-37-9 Usage

General Description

Ethyl 3-(N,N-dimethylamino)acrylate is a chemical compound with the molecular formula C8H15NO2. It is an ester derived from acrylic acid and N,N-dimethylamine. This colorless liquid is commonly used in the synthesis of polymers, adhesives, and coatings. It is also employed as a crosslinker in the production of resins and as a monomer in the manufacture of acrylic polymers. Ethyl 3-(N,N-dimethylamino)acrylate is considered to be a hazardous substance, with potential health hazards including eye and skin irritation, and it should be handled with caution in a controlled laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 1117-37-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1117-37:
(6*1)+(5*1)+(4*1)+(3*7)+(2*3)+(1*7)=49
49 % 10 = 9
So 1117-37-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO2/c1-4-10-7(9)5-6-8(2)3/h5-6H,4H2,1-3H3/b6-5+

1117-37-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 3-(N,N-Dimethylamino)Acrylate

1.2 Other means of identification

Product number -
Other names (E)-Ethyl 3-(dimethylamino)acrylate

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:1117-37-9 SDS

1117-37-9Relevant articles and documents

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Niederhauser,A.,Neuenschwander,M.

, p. 1318 - 1330 (1973)

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De Benneville,Macartney

, p. 3725 (1950)

Biaryl and atropisomeric biaryl aldehyde synthesis by one-step, metal-free benzannulation of aryl enals and propiolates

Hu, Deqing,Wan, Jie-Ping,Yang, Lu

, p. 6773 - 6777 (2020)

A new method involving the benzannulation of aromatic enals and two alkyl propiolate molecules has been developed as a powerful route to biaryl aldehydes simply via the promotion of dimethyl amine. The benzannulation process in the absence of an oxidant additive tolerates successfully the formyl group in the enal component, leading to a straightforward one-step synthesis of biaryl and atropisomeric aldehydes. An enamine activation based on the aza-Michael addition of dimethyl amine to the propiolate and the amine elimination-based generation of cyclohexadiene intermediate constitute the major factors enabling the titled reactions. This journal is

Preparation method of ethyl 3-(N,N-dimethylamino)acrylate

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Paragraph 0027-0044, (2021/02/10)

The invention relates to a preparation method of ethyl 3-(N,N-dimethylamino)acrylate, which comprises the following steps: carrying out heating reaction on formic acid, ethyl acetate and dimethylamineto obtain ethyl 3-(N,N-dimethylamino)acrylate and water. The preparation method of the ethyl 3-(N,N-dimethylamino)acrylate is short in reaction route, high in yield and purity and low in safety risk.

Synthesis method for N,N-dimethylaminoethyl acrylate

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Paragraph 0018; 0019; 0020; 0021; 0022; 0023-0038, (2017/07/21)

The invention discloses a synthesis method for N,N-dimethylaminoethyl acrylate. The method includes the following steps that 1, raw material preparation is carried out, wherein ethyl acetate, carbon monoxide, dimethylamine carbonate and sodium ethoxide serve as raw material; 2, material blending is carried out, wherein the molar ratio of ethyl acetate to carbon monoxide to dimethylamine carbonate to sodium ethoxide is (3-4):(0.9-1.1):(1.0-1.30):(1.2-1.4); 3, ethyl acetate, dimethylamine carbonate and sodium ethoxide are added into a vessel, carbon monoxide is introduced into the vessel, the temperature in the kettle is controlled to be 45-50 DEG C at the pressure of 0.2-0.8 MPa, and a heat-preserved reaction is carried out for 10 h; 4, after the reaction is finished, reduced pressure distillation is carried out to distill off a solvent, and the distilled solvent is recycled; 5, water is added into the vessel, standing is carried out for layering, an oil phase enters a rectification system, and N,N-dimethylaminoethyl acrylate is obtained through rectification. The product synthesized with the method contains few impurities, the amount of wastewater is small, the water resource is saved, the yield is high and reaches 5%, and the content is increased to 99.5% or above from 98%.

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