102336-07-2

Basic information

• Product Name: 4-Pyridinepropanoic acid, 2-methoxy-
• Synonyms: 4-Pyridinepropanoic acid, 2-methoxy-;3-(2-Methoxypyridin-4-Yl)Propanoic Acid;3-(2-Methoxypyridin-4-Yl)Propanoic Acid(WX613484)
• CAS NO: 102336-07-2
• Molecular Formula: C9H11NO3
• Molecular Weight: 181.19
• Mol File: 102336-07-2.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Pyridinepropanoic acid, 2-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Pyridinepropanoic acid, 2-methoxy-(102336-07-2)
• EPA Substance Registry System: 4-Pyridinepropanoic acid, 2-methoxy-(102336-07-2)

Safety Data

• Hazardous Substances Data: 102336-07-2(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
4-Pyridinepropanoic acid, 2-methoxy-, is used as a building block in organic synthesis for the creation of various biologically active molecules. Its unique structure and functional groups make it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
In pharmaceutical research, 4-Pyridinepropanoic acid, 2-methoxy-, serves as a key intermediate in the development of new drugs. Its ability to modulate biological processes and interact with various molecular targets makes it a promising candidate for drug discovery and optimization.
Used in Drug Development:
4-Pyridinepropanoic acid, 2-methoxy-, has potential therapeutic applications due to its ability to modulate biological processes. Researchers are exploring its potential as a drug candidate for the treatment of various diseases and conditions, making it a valuable asset in drug development.
Used in Agrochemical Production:
In the agrochemical industry, 4-Pyridinepropanoic acid, 2-methoxy-, is used as a reagent in the production of various agrochemicals. Its unique properties and functional groups make it suitable for the development of new pesticides, herbicides, and other agricultural chemicals.

Upstream product

• 119836-17-8 3-(2-methoxy-4-pyridyl)propionaldehyde diethyl acetal 
• 13466-41-6 4-methyl-1H-pyridin-2-one 
• 100848-70-2 2-methoxy-4-methyl-pyridine 
• 4926-28-7 2-Bromo-4-picoline 
• 3678-62-4 2-chloro-4-picoline 
• 695-34-1 2-Amino-4-methylpyridine 
• 119836-18-9 3-(2-methoxy-4-pyridyl)propionaldehyde 
• 3926-62-3 sodium monochloroacetic acid 

Downstream Products

• 170026-02-5 2-(2-methoxy-4-pyridyl)ethylamine dihydrochloride 
• 1401462-03-0 2-(2-methoxypyridin-4-yl)ethanamine hydrochloride 
• 170026-06-9 N-n-propyl-N-<2-(2-methoxy-4-pyridyl)ethyl>-2-phenylethanamide 
• 170026-09-2 N-propyl-N-(2-phenylethyl)-2-(2-methoxy-4-pyridyl)ethylamine 
• 764708-27-2 2-(2-methoxypyridin-4-yl)ethylamine 

Relevant articles and documents

DODECA-2E,4E-DIENE AMIDES AND THEIR USE AS MEDICAMENTS AND COSMETICS

The present invention relates to a novel class of compounds, namely dodeca-2E, 4E-diem amides and their use a medicament, preferably as a dermatologic agent, and as a cosmetic:. These novel compounds are particularly useful in treating and/or preventing inflammation, irritation, itching, pruritus, pain, oedema and/or pro-allergic or allergic conditions in a patient. Usually they are topically applied to the skin or mucosa in the form of a pharmaceutical or cosmetic composition comprising the compound and a pharmaceutically and/or cosmetically acceptable carrier.

THIAZOLOPYRIMIDINE COMPOUNDS

The present invention relates to the use of novel pyrrolopyrazine derivatives of formula I: wherein all variable substituents are defined as described herein, which are SYK inhibitors and are useful for the treatment of auto-immune and inflammatory diseases.

Synthesis of 2-Substituted 4-Pyridylpropionates. Part 2. Alkylation Approach

A synthesis of methyl 3-(2-methoxy-4-pyridyl)propionate (2), a key intermediate in the synthesis of the potent long-acting histamine H2-receptor antagonist SK&F 93574 (1), is described.The key step in the synthesis of compound (1) involves alkylation of 2-methoxy-4-methylpyridine (5) with sodium chloroacetate in the presence of sodamide.The scope and limitations of the alkylation is investigated using a variety of electrophiles.The application of this reaction to other 2-substituted 4-methylpyridines is also discussed.