166438-86-4

Basic information

• Product Name: 4-(4-METHYL-1,4-DIAZEPAN-1-YL)BENZALDEHYDE 97
• Synonyms: 4-(4-METHYL-1,4-DIAZEPAN-1-YL)BENZALDEHYDE;4-(4-METHYLPERHYDRO-1,4-DIAZEPIN-1-YL)BENZALDEHYDE;4-(4-METHYL-1,4-DIAZEPAN-1-YL)BENZALDEHYDE 97;4-(4-Methyl-1,4-diazepan-1-yl)benzaldehyde 97%;4-(4-Methylhomopiperazin-1-yl)benzaldehyde;4-(4-Methylhomopiperazin-1-yl)benzaldehyde, 1-(4-Formylphenyl)-4-methylhomopiperazine;4-(4-Methylhomopiperazin-1-yl)benzaldehyde97%
• CAS NO: 166438-86-4
• Molecular Formula: C13H18N2O
• Molecular Weight: 218.29482
• Mol File: 166438-86-4.mol
• Article Data: 3

Chemical Properties

• Melting Point: 44-46
• Boiling Point: 366.6°Cat760mmHg
• Flash Point: 160.1°C
• Appearance: /
• Density: 1.079g/cm³
• Vapor Pressure: 1.45E-05mmHg at 25°C
• Refractive Index: 1.567
• CAS DataBase Reference: 4-(4-METHYL-1,4-DIAZEPAN-1-YL)BENZALDEHYDE 97(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-METHYL-1,4-DIAZEPAN-1-YL)BENZALDEHYDE 97(166438-86-4)
• EPA Substance Registry System: 4-(4-METHYL-1,4-DIAZEPAN-1-YL)BENZALDEHYDE 97(166438-86-4)

Safety Data

• Hazard Codes: C
• Hazardous Substances Data: 166438-86-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H18N2O/c1-14-7-2-8-15(10-9-14)13-5-3-12(11-16)4-6-13/h3-6,11H,2,7-10H2,1H3

Upstream product

• 898289-58-2 [4-(4-methylperhydro-1,4-diazepin-1-yl)phenyl]methanol 
• 166438-80-8 4-(4-Methyl-1,4-diazepan-1-yl)benzonitrile 

Relevant articles and documents

A “universal” catalyst for aerobic oxidations to synthesize (hetero)aromatic aldehydes, ketones, esters, acids, nitriles, and amides

Functionalized (hetero)aromatic compounds are indispensable chemicals widely used in basic and applied sciences. Among these, especially aromatic aldehydes, ketones, carboxylic acids, esters, nitriles, and amides represent valuable fine and bulk chemicals, which are used in chemical, pharmaceutical, agrochemical, and material industries. For their synthesis, catalytic aerobic oxidation of alcohols constitutes a green, sustainable, and cost-effective process, which should ideally make use of active and selective 3D metals. Here, we report the preparation of graphitic layers encapsulated in Co-nanoparticles by pyrolysis of cobalt-piperazine-tartaric acid complex on carbon as a most general oxidation catalyst. This unique material allows for the synthesis of simple, functionalized, and structurally diverse (hetero)aromatic aldehydes, ketones, carboxylic acids, esters, nitriles, and amides from alcohols in excellent yields in the presence of air.

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.