74598-75-7

Basic information

• Product Name: 2,5-di-isopropylbenzaldehyde
• Synonyms: 2,5-di-isopropylbenzaldehyde
• CAS NO: 74598-75-7
• Molecular Weight: 190.285
• Mol File: 74598-75-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,5-di-isopropylbenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-di-isopropylbenzaldehyde(74598-75-7)
• EPA Substance Registry System: 2,5-di-isopropylbenzaldehyde(74598-75-7)

Safety Data

• Hazardous Substances Data: 74598-75-7(Hazardous Substances Data)

Upstream product

• 98-82-8 Isopropylbenzene 
• 201230-82-2 carbon monoxide 
• 100-18-5 1,4-bis(1-methylethyl)benzene 
• 4885-02-3 Dichloromethyl methyl ether 

Downstream Products

• 945971-89-1 2,5-di-isopropylbenzyl alcohol 
• 1558011-07-6 1-(2,5-diisopropylphenyl)ethanol 
• 1558011-11-2 C₃₄H₄₁ClNPPd 
• 1558011-10-1 (±)-trans-dichlorobis[1-(2,5-diisopropylphenyl)-N-methylethanamine]palladium(II) 
• 1558011-09-8 1-(2,5-diisopropylphenyl)-N,N-dimethylethanamine 
• 1558011-08-7 2-(1-bromoethyl)-1,4-diisopropylbenzene 
• 59424-70-3 1,4-Diisopropyl-2-[2,2,2-trichloro-1-(4-methoxy-phenyl)-ethyl]-benzene 
• 59424-92-9 2,2,2-Trichloro-1-(2,5-diisopropyl-phenyl)-ethanol 
• 177166-37-9 2,5-Diisopropylphenyl-tris(trimethylsilyl)methanol 

Relevant articles and documents

BENZODIAZEPINONE COMPOUNDS AND METHODS OF TREATMENT USING SAME

The invention provides 1,4-benzodiazepinone compounds, pharmaceutical compositions, and methods of treating autoimmune disorders, chronic inflammatory disorders, and hyperproliferative disorders. For example, the 1,4-benzodiazepinone compounds and pharmaceutical compositions are contemplated to be useful for treating rheumatoid arthritis, graft-versus-host disease, inflammatory bowel disease, and the like.

Paracyclophanes. Part 58 [1]. On the use of the stilbene-phenanthrene photocyclization in [2.2]paracyclophane chemistry

The application of the stilbene→phenanthrene photocyclization to [2.2]paracyclophane chemistry has been investigated. For the model system 4-styryl[2.2]paracyclophane (2) to [2.2]phenanthrenoparacyclophane (3) the reaction allows the introduction of alkyl substituants in the 6-, 7-, 8- and 9-position of the phenanthrene moiety. However, when the substituent in the 9-position (bay area of phenanthrene nucleus) becomes too large, viz. tert-butyl, no ring closure is observed anymore. The side products of the process (ring cleavage products of the cyclophane core such as 9 and 10) have been characterized for the first time. Extension of the condensed deck is possible leading to PAH-phanes as demonstrated by the preparation of the chrysenophanes 45 and 60; the cyclization to novel helicenophanes such as 50 also takes place without difficulties. In the case of 1,2-di(4-[2.2] paracyclophanyl)ethene (63) the triply-layered hydrocarbon 65 is produced on irradiation in small amounts.