406-91-7

Basic information

• Product Name: 4,4,4-Trifluorobutanoyl chloride
• Synonyms: 4,4,4-Trifluorobutanoyl chloride;4,4,4-trifluorobutyryl chloride
• CAS NO: 406-91-7
• Molecular Formula: C₄H₄ClF₃O
• Molecular Weight: 160.5221696
• Mol File: 406-91-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4,4,4-Trifluorobutanoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4,4-Trifluorobutanoyl chloride(406-91-7)
• EPA Substance Registry System: 4,4,4-Trifluorobutanoyl chloride(406-91-7)

Safety Data

• Hazardous Substances Data: 406-91-7(Hazardous Substances Data)

Usage

Uses

4,4,4-Trifluorobutyryl Chloride can be used in the preparation of hydrazide compounds with pyriproxyfen useful for pest control.

Upstream product

• 79-37-8 oxalyl dichloride 
• 406-93-9 4,4,4-trifluorobutyric acid 
• 371-26-6 ethyl 4,4,4-trifluorobutanoate 

Downstream Products

• 461-34-7 4,4,4-trifluorobutyroamide 
• 1071927-00-8 N-(3-(5-(3,5-dichlorophenyl)-4,5-dihydro-5-trifluoromethyl-isoxazol-3-yl)phenyl)-4,4,4-trifluoro-butanamide 
• 1259391-87-1 C₂₁H₃₂F₃NO₄Si 
• 1446359-66-5 C₂₁H₁₇F₄N₇O₂ 
• 1415406-06-2 N-{2-chloro-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]benzyl}-4,4,4-trifluorobutanamide 
• 1237587-67-5 C₂₇H₁₈Cl₃F₆N₃O₃ 
• 1237587-64-2 C₂₂H₁₆Cl₃F₆N₃O₃ 
• 1237587-42-6 N′-methyl-N′-{2-chloro-5-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}-4,4,4-trifluorobutyrohydrazide 
• 1237587-29-9 N′-{5-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-2-chlorophenyl}-4,4,4-trifluorobutyrohydrazide 
• 929612-39-5 1-phenyl-4-(4,4,4-trifluorobutyryloxy)-1,8-naphthyridin-2(1H)-one 
• 872549-86-5 5,5,5-trifluoro-1-[3-(methyloxy)phenyl]-2-pentanone 
• 136564-80-2 (4R,5S)-3-(1-oxo-4,4,4-trifluorobutyl)-4-methyl-5-phenyl-2-oxazolidinone 
• 460-39-9 3,3,3-trifluoropropylamine 

Relevant articles and documents

Antiviral compounds

A method of inhibiting lentivirus is disclosed which comprises mammalian host susceptible to said lentivirus with a virally inhibitory effective amount of an O-acylated derivative of 1,5-dideoxy-1,5-imino-D-glucitol and their N-alkyl, N-acyl and N-aroyl derivatives in which from one to four of the free hydroxyl groups are O-acylated with carboxylic alkanoyl radicals selected from the group consisting of ω,ω,ω-trifluoroalkanoyl having from three to eight carbon atoms, carboxylic cycloalkanoyl groups having from four to eight carbon atoms and carboxylic acyclic alkanoyl groups having from two to ten carbon atoms, wherein the N-aroyl groups contain from 7 to 14 carbon atoms, the N-acyl groups contain from 4 to 8 carbon atoms and the N-alkyl groups contain from 1 to 14 carbon atoms.

1,5-dideoxy-1,5-imino-d-glucitol derivatives

Antiviral O-acylated derivatives of 1,5-dideoxy-1,5-imino-D-glucitol are disclosed that contain an N-alkyl or N-aroyl radical in which from one to four of the free hydroxyl groups are O-acylated with carboxylic alkanoyl radicals selected from the group consisting of ω,ω,ω-trifluoro alkanoyl having from three to eight carbon atoms, carboxylic cycloalkanoyl groups having from four to eight carbon atoms and carboxylic acyclic alkanoyl groups having from two to ten carbon atoms, wherein the N-aroyl radical is selected from the group consisting of p-decylbenzoyl, 3-(p-chlorophenoxy)propanoyl, 2-(acetyloxy)benzoyl, [1,1'-biphenyl]-4-ylcarbonyl, 2-thiopheneacetyl, trans-3-furanacryloyl, 3-methoxyphenylacetyl and 3-(trifluoromethyl)benzoyl, and wherein the N-alkyl contains from one to fourteen carbon atoms, provided that when N-alkyl contains from one to five carbon atoms the O-acylated groups are ω,ω,ω-trifluoro alkanoyl or carboxylic cycloalkanoyl.