72965-00-5

Upstream product

• 1823-90-1 4-hydroxy-3,3-dimethyl-butan-2-one 
• 563-80-4 3-methyl-butan-2-one 
• 4301-02-4 3,3-dimethyl-4-[(methylsulphonyl)oxy]-2-butanone 

Downstream Products

• 1447941-22-1 di-tert-butyl(1S,1'S)-1,1'-(5,5'-(biphenyl-4,4'-diyl)bis(1H-imidazole-5,2-diyl))bis(3-fluoro-2,2-dimethylpropane-1,1-diyl)dicarbamate 

Relevant academic research and scientific papers

Hepatitis C Virus Inhibitors

The present disclosure is generally directed to antiviral compounds, and more specifically directed to combinations of compounds which can inhibit the function of the NS5A protein encoded by Hepatitis C virus (HCV), compositions comprising such combinations, and methods for inhibiting the function of the NS5A protein.

COMBINATIONS OF HEPATITIS C VIRUS INHIBITORS

The present disclosure is generally directed to antiviral compounds, and more specifically directed to combinations of compounds which can inhibit the function of the NS5A protein encoded by Hepatitis C virus (HCV), compositions comprising such combinations, and methods for inhibiting the function of the NS5A protein.

Combating fungi with substituted triazolylalkyl pyridyl ethers

Substituted triazolylalkyl pyridyl ethers of the formula STR1 in which R1 is a halogen atom, R2 is a hydrogen or halogen atom, X is a keto group or a CH(OH) group, Y each independently is a halogen atom or an alkyl, alkoxy or cyano group, and n is 0, 1, 2, 3 or 4, or an addition product thereof with a physiologically acceptable acid or metal salt which possesses fungicidal activity. Intermediates therefor wherein X is a keto group and with a halogen atom in place of either the pyridinyloxy group or the azole group are also new.

Combating fungi with acylated imidazolyl-gamma-fluoropinacolyl derivatives

Fungicidally active acylated imidazolyl-γ-fluoropiniacolyl derivatives of the formula STR1 in which R represents alkyl, alkenyl, alkynyl, alkoxy, alkoxyalkyl, cycloalkyl, halogenoalkyl, optionally substituted phenyl, optionally substituted phenylalkyl, op

Combating fungi with 1-phenoxy -1-imidazol-1-yl-4-fluoro-butane derivatives

1-Phenoxy-1-imidazol-1-yl-4-fluoro-butane derivatives of the formula STR1 in which B is --CO- or --CH(OH)--, X is hydrogen or fluorine, Z each independently is halogen, alkyl, nitro, cyano, alkoxy-carbonyl or optionally substituted phenyl, and n is 0, 1,

Combating fungi with 1-phenoxy-1-triazolyl-3-fluoromethyl-butane derivatives

1-Phenoxy-1-triazolyl-3-fluoromethyl-butane derivatives of the formula STR1 in which Az is 1,2,4-triazol-1-yl or 1,2,4-triazol-4-yl, B is --CO-- or --CH(OH)--, X is hydrogen or fluorine, Z each independently is halogen, alkyl, nitro, cyano, alkoxy-carbony

Combating arthropods with substituted 2-carbamoyloximino-butanes

Substituted 2-carbamoyloximino-butanes of the formula STR1 in which R is alkyl or alkylthioalkyl, R1 is alkyl, alkoxyalkyl, alkenyl or alkynyl, R2 is hydrogen, alkyl or --SR3, R3 is alkyl, halogenoalkyl, optionally substituted phenyl, alkoxycarbonyl, --N(CH3)R4, or a radical identical to that to which --SR3 is bonded, R4 is alkyl, alkoxycarbonyl or optionally substituted phenylsulphonyl, X is hydrogen or halogen, Y is hydrogen or halogen, Z is halogen, and n is 0, 1 or 2, which possess arthropodicidal activity.

Acylated triazolyl-γ-fluoropinacolyl derivatives and their use as fungicides

Fungicidally active acylated triazolyl-γ-fluoropinacolyl derivatives of the formula STR1 in which Az represents 1,2,4-triazol-1-yl or 1,2,4-triazol-4-yl, R represents alkyl, alkenyl, alkynyl, alkoxy, alkoxyalkyl, cycloalkyl, halogenoalkyl, optionally subs

Preparation of side-chain fluorinated 3,3-dimethyl-butan-2-one

A fluorine derivative of 3,3-dimethyl-butan-2-one, of the formula STR1 in which X is hydrogen or fluorine, is produced by reacting a metal fluoride in a diluent and at elevated temperature with a sulphonic acid ester of the formula STR2 in which R is opti