945971-89-1

Basic information

• Product Name: 2,5-di-isopropylbenzyl alcohol
• Synonyms: 2,5-di-isopropylbenzyl alcohol
• CAS NO: 945971-89-1
• Molecular Weight: 192.301
• Mol File: 945971-89-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,5-di-isopropylbenzyl alcohol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-di-isopropylbenzyl alcohol(945971-89-1)
• EPA Substance Registry System: 2,5-di-isopropylbenzyl alcohol(945971-89-1)

Safety Data

• Hazardous Substances Data: 945971-89-1(Hazardous Substances Data)

Upstream product

• 74598-75-7 2,5-di-isopropylbenzaldehyde 
• 42196-29-2 2-bromo-1,4-diisopropylbenzene 
• 100-18-5 1,4-bis(1-methylethyl)benzene 
• 57988-33-7 2,5-diisopropylbenzoic acid 

Downstream Products

• 945971-90-4 2,5-di-isopropylbenzyl bromide 
• 85995-32-0 α-(2,5-diisopropylphenyl)acetophenone 
• 137668-42-9 1,1-dimethyl-2-phenyl-2-hydroxy-5-isopropylindan 
• 58502-84-4 2,5-diisopropylbenzyl chloride 

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.