42580-35-8

Usage

Uses

Used in Chemical Synthesis:
4-(3-methoxypropoxy)benzaldehyde is used as a synthetic intermediate for the production of various organic compounds. Its unique structure allows it to be a key component in the synthesis of complex molecules, particularly in the pharmaceutical and chemical industries.
Used in Research and Development:
4-(3-methoxypropoxy)benzaldehyde is used as a research compound for studying its chemical properties and potential applications. Its reactivity and the ability to form various derivatives make it a valuable tool in the development of new materials and compounds.
Used in Pharmaceutical Industry:
4-(3-methoxypropoxy)benzaldehyde is used as a building block in the synthesis of pharmaceutical compounds. Its presence in the molecular structure can influence the biological activity and properties of the final drug product, making it an important component in drug discovery and development.
Used in Flavor and Fragrance Industry:
4-(3-methoxypropoxy)benzaldehyde is used as a component in the creation of unique fragrances and flavors. Its aromatic properties can contribute to the overall scent profile of a product, making it a valuable asset in the development of new fragrances and flavorings.

InChI:InChI=1/C11H14O3/c1-13-7-2-8-14-11-5-3-10(9-12)4-6-11/h3-6,9H,2,7-8H2,1H3

Upstream product

• 17954-81-3 4-(3-bromopropoxy)benzaldehyde 
• 124-41-4 sodium methylate 
• 123-08-0 4-hydroxy-benzaldehyde 

Downstream Products

• 1184361-77-0 [4-(3-methoxypropoxy)phenyl]methanol 
• 1422064-30-9 methyl 1-[4-(3-methoxypropoxy)benzyl]-5-oxo-L-prolinate 
• 1422064-39-8 1-[4-(3-methoxypropoxy)benzyl]-5-oxo-L-prolyl-L-histidine 
• 1422064-33-2 1-[4-(3-methoxypropoxy)benzyl]-5-oxo-L-proline 
• 1422064-36-5 benzyl 1-[4-(3-methoxypropoxy)benzyl]-5-oxo-L-prolyl-3-trityl-L-histidinate 

Relevant academic research and scientific papers

PIPERIDINE-DIONE DERIVATIVES

The invention provides novel compounds having the general formula (I) and tautomers and pharmaceutically acceptable salts thereof, wherein A1, A2, A3, A4, R1, R4, R5, R6, R7 and R8 are as defined herein, compositions including the compounds and methods of using the compounds.

Synthesis of new optically active 2-pyrrolidinones

A new class of optically active 2-pyrrolidinones was synthesized, starting from S-pyroglutamic acid, a well known natural chiral synthon. The synthetic design followed led to the insertion of various substituents at positions 1 and 5 of the 2-pyrrolidinone ring, including the imidazole moiety. Some of them possess two or three stereogenic centers, the configuration of which was retained under the mild conditions used. The new compounds also carry an imidazole moiety, which, along with the 2-pyrrolidinone template, may prove pivotal to several biological processes.

SUBSTITUTED 1-AMINOPHTHALAZINE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC APPLICATION THEREOF

The invention concerns 1-amino-phthalazine derivatives of general formula (I): Wherein A, B, L, R, R1, R2, R3, R4, R5 and R7 are as defined herein. The invention also concerns the preparation of said compounds and their therapeutic use.

Imidazole derivatives

The present invention relates to the imidazole derivative of the following formula (I) wherein R1 is hydrogen, optionally substituted alkyl and the like, R2 is hydrogen, optionally substituted alkyl and the like, R3is optionally substituted heteroaryl, R4 is optionally substituted cycloalkyl, optionally substituted phenyl and the like, provided that when R1 is hydrogen, and R2 and R4 are the same or different and each is phenyl or phenyl substituted by halogen atom, lower alkyl or lower alkoxy, R3 is benzothiazolyl or thiazolyl substituted by phenyl, the imidazole derivative of the following formula (XII) wherein R6 is optionally substituted phenyl or optionally substituted heteroaryl and R7 is substituted phenyl, and pharmaceutically acceptable salts thereof. The compounds of the formulas (I) and (XII) and pharmaceutically acceptable salts thereof of the present invention inhibit IL-4 and IL-5 production by Th2 cells and are effective for the prophylaxis and treatment of allergic diseases such as atopic dermatitis, bronchial asthma, allergic rhinitis and the like.