2-ETHYL-9,10-DIMETHOXYANTHRACENE

2-ETHYL-9,10-DIMETHOXYANTHRACENE Structure
2-ETHYL-9,10-DIMETHOXYANTHRACENE structure
Common Name 2-ETHYL-9,10-DIMETHOXYANTHRACENE
CAS Number 26708-04-3 Molecular Weight 266.33400
Density 1.116g/cm3 Boiling Point 435.2ºC at 760 mmHg
Molecular Formula C18H18O2 Melting Point 117-119ºC(lit.)
MSDS USA Flash Point 177.6ºC
Symbol GHS08 GHS09
GHS08, GHS09
Signal Word Danger

Application of a mathematical topological pattern of antihistaminic activity for the selection of new drug candidates and pharmacology assays.

J. Med. Chem. 49(12) , 3667-73, (2006)

Molecular topology was used to achieve a mathematical model capable of classifying compounds according to their antihistaminic activity and low sedative effects. By application of this model of activity to databases containing chemical reagents and drugs exhi...

Quantum yields lower than unity in photo- induced dissociative electron transfers: the reductive cleavage of carbon tetrachloride.

ChemPhysChem 1(4) , 199-205, (2000)

It has been shown recently that the electrochemical reduction of carbon tetrachloride in N,N'-dimethylformamide follows a mechanism in which electron transfer and bond cleavage are concerted. We report here results concerning photoinduced electron transfer fr...

Photocationic and radical polymerizations of epoxides and acrylates by novel sulfonium salts. Takahashi E, et al.

J. Polym. Sci. A Polym. Chem. 41(23) , 3816-27, (2003)

Photosensitized reduction of sulfonium salts: Evidence for nondissociative electron transfer. Wang X, et al.

J. Am. Chem. Soc. 121(8) , 4364-68, (1999)

Novel N-methylbenzothiazolium salts as hardeners for epoxy and acrylate monomers. Takahashi E, et al.

J. Polym. Sci. A Polym. Chem. 41(23) , 3828-37, (2003)

Anthracene electron-transfer photosensitizers for onium salt induced cationic photopolymerizations. Crivello JV and Jang M.

J. Photochem. Photobiol. A: Chem. 159(2) , 173-188, (2003)

Stepwise and concerted pathways in photoinduced and thermal electron-transfer/bond-breaking reactions. Experimental illustration of similarities and contrasts. Pause L, et al.

J. Am. Chem. Soc. 123(21) , 4886-4895, (2001)