660423-00-7

Usage

Uses

Used in Pharmaceutical Industry:
4-(tert-butoxy)-3,3-diMethyl-4-oxobutanoic acid is used as a synthetic intermediate for the production of various chemical compounds with therapeutic activity. Its versatile chemical structure allows it to be a key component in the synthesis of a wide range of pharmaceuticals, including Betulin derivatives, which have potential applications in the treatment of various diseases.
Used in Chemical Synthesis:
In the field of chemical synthesis, 4-(tert-butoxy)-3,3-diMethyl-4-oxobutanoic acid serves as a valuable building block for creating a diverse array of compounds. Its reactivity and functional groups make it a useful starting material for the development of new molecules with potential applications in various industries, such as pharmaceuticals, agrochemicals, and materials science.
Used in Research and Development:
4-(tert-butoxy)-3,3-diMethyl-4-oxobutanoic acid is also utilized in research and development settings, where it can be employed to study the properties and reactivity of various chemical compounds. Its unique structure and functional groups make it an interesting subject for exploring new reaction pathways and developing innovative synthetic methods.

Upstream product

• 660422-99-1 1-tert-butyl 4-ethyl 2,2-dimethylsuccinate 
• 17347-61-4 2,2-dimethylsuccinic anhydride 
• 121925-55-1 4-ethoxy-2,2-dimethyl-4-oxobutanoic acid 

Downstream Products

• 1422355-59-6 4-((3aR,5aR,5bR,7aR,9S,11aR,11bR,13aS)-3a-(2-(1-(4-chlorophenyl)-cyclopropylamino)-2-oxoacetyl)-1-isopropyl-5a,5b,8,8,11a-pentamethyl-2-oxo-3,3a,4,5,5a,5b,6,7,7a,8,9,10,11,11a,11b,12,13,13a-octadecahydro-2H-cyclopenta[a]chrysen-9-yloxy)-2,2-dimethyl-4-oxobutanoic acid 
• 1422355-61-0 (1R,2R,5R,10S,13R,14R,17S,19R)-5-({[1-(4-chlorophenyl)cyclopropyl]carbamoyl}(oxo)methyl)-1,2,14,18,18-pentamethyl-7-oxo-8-(propan-2-yl)pentacyclo[11,8.0.0^2,10.0^5,9.0^14,19]henicos-8-en-17-yl 1-(2-hydroxyethyl)2,2-dimethylbutanedioate 
• 1422355-62-1 {[(4-{[(1R,2R,5R,10S,13R,14R,17S,19R)-5-({[1-(4-chlorophenyl)cyclopropyl]carbamoyl}(oxo)methyl)-1,2,14,18,18-pentamethyl-7-oxo-8-(propan-2-yl)pentacyclo[11.8.0.0^2,10.0^5,9.0^14,19]henicos-8-en-17-yl]oxy}-2,2-dimethyl-4-oxobutanoyl)oxy]methoxy}phosphonic acid 
• 1422356-80-6 C₅₅H₈₁ClNO₁₁P 
• 1422355-63-2 {2-[(4-{[(1R,2R,10S,13S,14R,17S,19R)-5-({[1-(4-chlorophenyl)cyclopropyl]carbamoyl}(oxo)methyl)-1,2,14,18,18-pentamethyl-7-oxo-8-(propan-2-yl)pentacyclo[11.8.0.0^2,10.0^5,9.0^14,19]henicos-8-en-17-yl]oxy}-2,2-dimethyl-4-oxobutanoyl)oxy]ethoxy}phosphonic acid 
• 1422356-81-7 C₅₆H₈₃ClNO₁₁P 
• 1443513-44-7 1-tert-butyl 4-((3aS,5aR,5bR,7aR,9S,11aR,11bR,13aS)-3a-((E)-3-((1-(4-chlorophenyl)cyclopropyl)amino)-2-methyl-3-oxoprop-1-en-1-yl)-1-isopropyl-5a,5b,8,8,11a-pentamethyl-2-oxo-3,3a,4,5,5a,5b,6,7,7a,8,9,10,11,11a,11b,12,13,13a-octadecahydro-2H-cyclopenta[a]chrysen-9-yl) 2,2-dimethylsuccinate 
• 1443513-22-1 4-(((3aS,5aR,5bR,7aR,9S,11aR,11bR,13aS)-3a-((E)-3-((1-(4-chlorophenyl)cyclopropyl)amino)-2-methyl-3-oxoprop-1-en-1-yl)-1-isopropyl-5a,5b,8,8,11a-pentamethyl-2-oxo-3,3a,4,5,5a,5b,6,7,7a,8,9,10,11,11a,11b,12,13,13a-octadecahydro-2H-cyclopenta[a]chrysen-9-yl)oxy)-2,2-dimethyl-4-oxobutanoic acid 
• 1443513-48-1 1-tert-butyl 4-((3aR,5aR,5bR,7aR,9S,11aR,11bR,13aS)-3a-((E)-3-(((S)-1-(3-chlorophenyl)ethyl)amino)-3-oxoprop-1-en-1-yl)-1-isopropyl-5a,5b,8,8,11a-pentamethyl-3,3a,4,5,5a,5b,6,7,7a,8,9,10,11,11a,11b,12,13,13a-octadecahydro-2H-cyclopenta[a]chrysen-9-yl) 2,2-dimethylsuccinate 
• 1443513-29-8 4-(((3aS,5aR,5bR,7aR,9S,11aR,11bR,13aS)-3a-((E)-3-(((S)-1-(3-chorophenyl)ethyl)amino)-3-oxoprop-1-en-1-yl)-1-isopropyl-5a,5b,8,8,11a-pentamethyl-3,3a,4,5,5a,5b,6,7,7a,8,9,10,11,11a,11b,12,13,13a-octadecahydro-2H-cyclopenta[a]chrysen-9-yl)oxy)-2,2-dimethyl-4-oxobutanoic acid 
• 1443513-38-9 1-tert-butyl 4-((3aS,5aR,5bR,7aR,9S,11aR,11bR,13aS)-3a-((E)-3-((1-(4-chlorophenyl)cyclopropyl)amino)-3-oxoprop-1-en-1-yl)-1-isopropyl-5a,5b,8,8,11a-pentamethyl-2-oxo-3,3a,4,5,5a,5b,6,7,7a,8,9,10,11,11a,11b,12,13,13a-octadecahydro-2H-cyclopenta[a]chrysen-9-yl) 2,2-dimethylsuccinate 
• 1449796-61-5 C₄₇H₆₇ClN₄O₅ 
• 1449796-62-6 C₄₆H₆₅ClN₄O₅ 
• 1449796-60-4 C₄₇H₆₇ClN₄O₅ 

Relevant academic research and scientific papers

NOVEL COMPOUNDS FOR CONTROLLING ARTHROPODS

The present invention relates to novel halogen-substituted compounds, to processes for their preparation and to their use for controlling animal pests, in particular arthropods and especially insects and arachnids.

CARBONYL DERIVATIVES OF BETULIN

Disclosed are a compound characterized by the following formula I or a pharmaceutically acceptable salt thereof, and a pharmaceutical composition comprising said compound or a pharmaceutically acceptable salt thereof, wherein R3, L, and A are as described in the application. Said compounds are useful for the treatment of HIV.

PROPENOATE DERIVATIVES OF BETULIN

The present invention relates to a compound characterized by the following Formula I or a pharmaceutically acceptable salt thereof, wherein X, Y, and Z are as described herein. Compounds of the present invention are useful for the treatment of HIV.

DERIVATIVES OF BETULIN

The present invention relates to compounds characterized by having a structure according to the following Formula I: (I), or a pharmaceutically acceptable salt thereof. Compounds of the present invention are useful for the treatment or prevention of HIV.

PROPENOATE DERIVATIVES OF BETULIN

The present invention relates to a compound characterized by Formula (I); or a pharmaceutically acceptable salt thereof, wherein X, Y, and Z are as described herein. Compounds of the present invention are useful for the treatment of HIV.

NEW COMPOUNDS

The present invention relates to new compounds of formula I, (I) a process for their preparation and new intermediates prepared therein, pharmaceutical formulations containing said compounds and to the use of said compounds in therapy.