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(6-CHLORO-PYRIDIN-3-YL)-OXO-ACETIC ACID ETHYL ESTER is a chemical compound with the molecular formula C9H8ClNO3. It is a derivative of pyridine, featuring a chloro substituent on the third carbon atom and an ethyl ester group attached to the oxo-acetic acid moiety. (6-CHLORO-PYRIDIN-3-YL)-OXO-ACETIC ACID ETHYL ESTER is primarily utilized as an intermediate in organic synthesis, particularly for the production of pharmaceuticals and agrochemicals. Its ability to undergo various chemical reactions allows it to form complex molecules with diverse biological activities, making it significant for the development of new materials and scientific research.

902837-55-2

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902837-55-2 Usage

Uses

Used in Pharmaceutical Industry:
(6-CHLORO-PYRIDIN-3-YL)-OXO-ACETIC ACID ETHYL ESTER is used as a synthetic intermediate for the development of pharmaceuticals. Its unique structure and reactivity enable the creation of complex molecules with potential therapeutic properties, contributing to the advancement of new drug candidates.
Used in Agrochemical Industry:
In the agrochemical sector, (6-CHLORO-PYRIDIN-3-YL)-OXO-ACETIC ACID ETHYL ESTER serves as a key intermediate in the synthesis of various agrochemicals. Its involvement in the production process helps in developing effective compounds for crop protection and pest management.
Used in Material Science:
(6-CHLORO-PYRIDIN-3-YL)-OXO-ACETIC ACID ETHYL ESTER is utilized in material science for the development of new materials. Its chemical properties allow for the formation of novel structures with unique characteristics, expanding the scope of material applications in various industries.
Used in Scientific Research:
(6-CHLORO-PYRIDIN-3-YL)-OXO-ACETIC ACID ETHYL ESTER is also important in scientific research, where it is employed to study various chemical reactions and explore its potential applications in different fields. Its versatility and reactivity make it a valuable tool for researchers working on innovative projects and discoveries.

Check Digit Verification of cas no

The CAS Registry Mumber 902837-55-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,2,8,3 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 902837-55:
(8*9)+(7*0)+(6*2)+(5*8)+(4*3)+(3*7)+(2*5)+(1*5)=172
172 % 10 = 2
So 902837-55-2 is a valid CAS Registry Number.
InChI:InChI=1S/C9H8ClNO3/c1-2-14-9(13)8(12)6-3-4-7(10)11-5-6/h3-5H,2H2,1H3

902837-55-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H50157)  Ethyl 2-chloro-5-pyridylglyoxylate, 97%   

  • 902837-55-2

  • 1g

  • 1240.0CNY

  • Detail

  • Alfa Aesar

  • (H50157)  Ethyl 2-chloro-5-pyridylglyoxylate, 97%   

  • 902837-55-2

  • 5g

  • 7097.0CNY

  • Detail

902837-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(6-chloropyridin-3-yl)-2-oxoacetate

1.2 Other means of identification

Product number -
Other names ETHYL (6-CHLOROPYRIDIN-3-YL)(OXO)ACETATE

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:902837-55-2 SDS

902837-55-2Downstream Products

902837-55-2Relevant academic research and scientific papers

Structure-activity relationship studies of novel 3-oxazolidinedione-6- naphthyl-2-pyridinones as potent and orally bioavailable EP3 receptor antagonists

Morales-Ramos, ángel I.,Li, Yue H.,Hilfiker, Mark,Mecom, John S.,Eidam, Patrick,Shi, Dongchuan,Tseng, Pei-San,Brooks, Carl,Zhang, David,Wang, Ning,Jaworski, Jon-Paul,Morrow, Dwight,Fries, Harvey,Edwards, Richard,Jin, Jian

, p. 2806 - 2811 (2011)

Multiple regions of the 3-oxazolidinedione-6-naphthyl-pyridinone series identified via high throughput screening were explored. SAR studies of these regions including the left-hand side oxazolidinedione moiety, α-substituent on the oxazolidinedione ring,

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