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3-(2-chloro-pyridin-4-yl)-acrylic acid ethyl ester is a chemical compound characterized by the presence of a 3-(2-chloro-pyridin-4-yl) group attached to an acrylic acid ethyl ester. 3-(2-CHLORO-PYRIDIN-4-YL)-ACRYLIC ACID ETHYL ESTER is known for its potential applications in pharmaceutical research and drug development, serving as an intermediate in the synthesis of various medications.

551950-41-5

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551950-41-5 Usage

Uses

Used in Pharmaceutical Industry:
3-(2-chloro-pyridin-4-yl)-acrylic acid ethyl ester is used as a chemical intermediate for the synthesis of various drugs, contributing to the development of new medications for a range of medical conditions.
Used in Drug Development:
3-(2-CHLORO-PYRIDIN-4-YL)-ACRYLIC ACID ETHYL ESTER is utilized in the research and development of new pharmaceuticals, with its unique structure offering potential therapeutic benefits in treating different health issues.
It is crucial to handle 3-(2-chloro-pyridin-4-yl)-acrylic acid ethyl ester with care due to its potential harmful effects if not properly managed, ensuring safety in pharmaceutical research and production processes.

Check Digit Verification of cas no

The CAS Registry Mumber 551950-41-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,1,9,5 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 551950-41:
(8*5)+(7*5)+(6*1)+(5*9)+(4*5)+(3*0)+(2*4)+(1*1)=155
155 % 10 = 5
So 551950-41-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H10ClNO2/c1-2-14-10(13)4-3-8-5-6-12-9(11)7-8/h3-7H,2H2,1H3/b4-3+

551950-41-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (E)-3-(2-chloropyridin-4-yl)prop-2-enoate

1.2 Other means of identification

Product number -
Other names -

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:551950-41-5 SDS

551950-41-5Upstream product

551950-41-5Downstream Products

551950-41-5Relevant articles and documents

Dimethyl sulfoxide mediated elimination reactions in 3-aryl 2,3-dihalopropanoates: Scope and mechanistic insights

Li, Wei,Li, Jianchang,Lin, Melissa,Wacharasindhu, Sumrit,Tabei, Keiko,Mansour, Tarek S.

, p. 6016 - 6021 (2008/02/10)

(Chemical Equation Presented) Dimethyl sulfoxide (DMSO) efficiently causes the reductive elimination of 3-aryl 2,3-dibromopropanoates to cinnamates with good yield. With 3-phenyl 2,3-dihalopropanoates, debromination is the major pathway providing 3-phenylacrylate derivatives in high yields, whereas dehydrobromination is a competing pathway with thiophene derivatives. 1H NMR, 81Br NMR, and MS techniques indicated the formation of brominated-DMSO, MeBr, and HBr as byproducts in this transformation with no evidence for the formation of Br2. The dual role of DMSO as a nucleophile and bromine scavenger accounts for the products formed in this reaction.

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