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ETHYL 3-(2-AMINOPYRIDIN-3-YL)ACRYLATE, a chemical compound with the molecular formula C11H12N2O2, is a yellow to brown solid with a molecular weight of 204.22 g/mol. It is an acrylate derivative that features a 3-(2-aminopyridin-3-yl) acrylate group, which endows it with unique structural properties. ETHYL 3-(2-AMINOPYRIDIN-3-YL)ACRYLATE is commonly utilized in the synthesis of pharmaceuticals, agrochemicals, and organic materials, and may hold potential applications in medicinal chemistry and biological research.

104830-01-5

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104830-01-5 Usage

Uses

Used in Pharmaceutical Synthesis:
ETHYL 3-(2-AMINOPYRIDIN-3-YL)ACRYLATE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the formation of complex molecular structures that can exhibit therapeutic effects.
Used in Agrochemical Production:
In the agrochemical industry, ETHYL 3-(2-AMINOPYRIDIN-3-YL)ACRYLATE is used as a building block in the creation of compounds that can be applied in crop protection and pest management, leveraging its reactivity and structural attributes to enhance the effectiveness of these products.
Used in Organic Material Synthesis:
ETHYL 3-(2-AMINOPYRIDIN-3-YL)ACRYLATE is utilized as a component in the synthesis of organic materials, where its unique group can influence the properties of the final materials, such as their reactivity, stability, or specific functional characteristics.
Used in Medicinal Chemistry Research:
ETHYL 3-(2-AMINOPYRIDIN-3-YL)ACRYLATE is employed as a research compound in medicinal chemistry to explore its potential interactions with biological targets, which could lead to the discovery of new drugs or therapeutic agents.
Used in Biological Research:
In biological research, ETHYL 3-(2-AMINOPYRIDIN-3-YL)ACRYLATE may be used to study its effects on biological systems, including potential uses in the development of bioactive molecules or understanding its interactions with cellular components.
Further studies are necessary to fully understand the potential uses and effects of ETHYL 3-(2-AMINOPYRIDIN-3-YL)ACRYLATE, as its unique structural properties could offer novel applications across various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 104830-01-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,3 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 104830-01:
(8*1)+(7*0)+(6*4)+(5*8)+(4*3)+(3*0)+(2*0)+(1*1)=85
85 % 10 = 5
So 104830-01-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O2/c1-2-14-9(13)6-5-8-4-3-7-12-10(8)11/h3-7H,2H2,1H3,(H2,11,12)

104830-01-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H50018)  Ethyl 3-(2-amino-3-pyridyl)acrylate, 95%   

  • 104830-01-5

  • 1g

  • 1829.0CNY

  • Detail
  • Alfa Aesar

  • (H50018)  Ethyl 3-(2-amino-3-pyridyl)acrylate, 95%   

  • 104830-01-5

  • 5g

  • 7833.0CNY

  • Detail

104830-01-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-(2-aminopyridin-3-yl)prop-2-enoate

1.2 Other means of identification

Product number -
Other names Ethyl4-amino-3-pyridineacrylate

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:104830-01-5 SDS

104830-01-5Downstream Products

104830-01-5Relevant academic research and scientific papers

Condensed Heteroaromatic Ring Systems. IV. Synthesis of Naphthyridine Derivatives by Cyclization of Aminopyridineacrylic Esters

Sakamoto, Takao,Kondo, Yoshinori,Yamanaka, Hiroshi

, p. 4764 - 4768 (2007/10/02)

The reaction of aminohalopyridines with ethyl acrylate in the presence of palladium(II)acetate and triarylphosphine gave ethyl aminopyridineacrylates.The cyclization of the resulting acrylates under basic conditions gave naphthyridinones having a carbostyril-type moiety.Keywords- intramolecular cyclization; palladium catalyst; ethyl acrylate; naphthyridinone; pyridineacrylic ester

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