129047-61-6

Basic information

• Product Name: 1-(4-Benzoylphenoxy)-10-bromodecane
• Synonyms: 1-(4-Benzoylphenoxy)-10-bromodecane
• CAS NO: 129047-61-6
• Molecular Weight: 417.386
• Mol File: 129047-61-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-(4-Benzoylphenoxy)-10-bromodecane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-Benzoylphenoxy)-10-bromodecane(129047-61-6)
• EPA Substance Registry System: 1-(4-Benzoylphenoxy)-10-bromodecane(129047-61-6)

Safety Data

• Hazardous Substances Data: 129047-61-6(Hazardous Substances Data)

Upstream product

• 4101-68-2 1,10-dibromodecane 
• 1137-42-4 4-Hydroxybenzophenone 

Downstream Products

• 129047-62-7 1-(4-Benzoylphenoxy)-10-<4-(phenylamino)phenoxy>decane 

Relevant articles and documents

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Substituted aminoalkoxybenzene anti-fungicidal compositions and use

The compound of the formula STR1 wherein each of R1 and R2 individually is hydrogen, lower alkyl or lower alkenyl or together signify straight-chain alkylene with 2 to 4 carbon atoms, R3 is hydrogen, halogen or lower alkyl, Q is alkylene with 4 to 11 carbon atoms and at least 4 carbon atoms between the two free valencies or alkenylene with 4 to 11 carbon atoms and at least 4 carbon atoms between the two free valencies and each of Y and Y' individually is a direct bond or the group --CH2 --, --CH2 CH2 --, --CH=CH-- or --C C--, the group R1 R2 N--Q--O-- is attached to the 3- or 4 -position of ring A and the symbol R designates that the ring to which it is attached is unsubstituted or is substituted with at least one substitutent selected from the group consisting of halogen, trifluoromethyl, cyano, nitro, lower alkyl and lower alkoxy, and their pharmaceutically acceptable acid addition salts can be used for the control or prevention of fungal infections, especially of topical or systemic infections which are caused by pathogenic fungi, and for the manufacture of antifungally-active medicaments. The compounds of formula I have not only a pronounced antifungal activity, but they also exhibit synergistic effects in combination with other known antifungally-active substances which inhibit sterol biosynthesis such as ketoconazole and terbinafine.