4415-84-3

Basic information

• Product Name: CYCLOBUTANEPROPANOIC ACID
• Synonyms: CYCLOBUTANEPROPANOIC ACID;3-cyclobutylpropanoic acid(SALTDATA: FREE);3-cyclobutylpropanoic acid;3-CYCLOBUTANEPROPANOIC ACID
• CAS NO: 4415-84-3
• Molecular Formula: C₇H₁₂O₂
• Molecular Weight: 128.16898
• Mol File: 4415-84-3.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: CYCLOBUTANEPROPANOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: CYCLOBUTANEPROPANOIC ACID(4415-84-3)
• EPA Substance Registry System: CYCLOBUTANEPROPANOIC ACID(4415-84-3)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 4415-84-3(Hazardous Substances Data)

Usage

Description

CYCLOBUTANEPROPANOIC ACID is an organic compound that features a cyclobutane ring fused to a propanoic acid structure. It is known for its unique chemical properties and potential applications in various fields, particularly in the pharmaceutical industry.

Uses

Used in Pharmaceutical Industry:
CYCLOBUTANEPROPANOIC ACID is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of novel drugs with specific therapeutic properties.
Used in the Preparation of Substituted Oxopyridine Derivatives:
CYCLOBUTANEPROPANOIC ACID is used as a starting material for the preparation of substituted oxopyridine derivatives, which are known to act as inhibitors of factor XIa and plasma kallikrein. These inhibitors have potential applications in the treatment of various medical conditions, such as coagulation disorders and inflammation.

Upstream product

• 14085-86-0 3-cyclobutylpropanenitrile 
• 4415-82-1 cyclobutanemethanol 
• 1010422-67-9 2-cyclobutylmethyl malonic acid 
• 36206-72-1 2-cyclobutylethyl 4-methylbenzenesulfonate 
• 13295-53-9 cyclobutylmethyl 4-methylbenzenesulfonate 
• 17247-58-4 (Bromomethyl)cyclobutane 
• 21782-47-8 ethyl 3-cyclobutyl-2-ethoxycarbonylpropionate 

Downstream Products

• 21782-48-9 3-(cyclobutyl)-1-propanol 
• 1455038-64-8 1-(5-(7-chloro-2-methyl-1,6-naphthyridin-3-yl)-2-fluoro-4-methylphenyl)-3-(2-cyclobutylethyl)urea 
• 71037-57-5 3-Cyclobutyl-propionyl chloride 
• 85390-03-0 3-Cyclobutyl-N-{2-[4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenyl]-ethyl}-propionamide 

Relevant articles and documents

QUINOLINE DERIVATIVES AS INHIBITORS OF AXL/MER RTK AND CSF1R

The present invention relates to quinoline derivatives which are inhibitors for Axl/Mer RTK (receptor tyrosine kinase) and CSF1R (colony stimulating factor 1 receptor). These compounds are suitable for the treatment of disorders associated with, accompanied by, caused by or induced by Axl/Mer RTK and CSF1R, in particular a hyperfunction thereof. The compounds are suitable for the treatment of hyperproliferative disorders, such as cancer, particularly immune-suppressive cancer (such as those cancers with an immunosuppression of innate immunity in a tumor microenvironment (TME), refractory cancer and cancer metastases. They are also useful in the treatment of inflammatory diseases and/or neurodegenerative diseases.

Practical synthesis of a peptide deformylase (PDF) inhibitor

A practical chromatography-free synthesis of an N-formylated hydroxylamine peptide deformylase inhibitor LCD320 is described. A diastereoselective Michael reaction of (4S)-3-[2-(cyclobutylmethyl)-l-oxo-2-propenyl]-4-(phenylmethyl)-2- oxazolidinone with 0-benzyl hydroxylamine was used to establish the key stereogenic center. We found that traces of residual Li+ from a previous step had a great impact on the diastereoselectivity of this reaction. A very efficient amidalion coupling reaction of proline derivative (2S,4R)-4-fluoro-1,2-m-pyrrolidinedicarboxylic acid 1,1-dimethylethyl ester with weakly nucleophilic 3-pyridazinamine using methanesulfonyl chloride in the presence of l-methylimidazole in DMF was also developed that proceeded without racemization.

Structure activity relations in acids related to cyclobutanecarboxylic acid

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