104115-44-8

Basic information

• Product Name: (2-oxocyclopent)acetic acid
• Synonyms: (2-oxocyclopent)acetic acid
• CAS NO: 104115-44-8
• Molecular Weight: 142.155
• Mol File: 104115-44-8.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: (2-oxocyclopent)acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (2-oxocyclopent)acetic acid(104115-44-8)
• EPA Substance Registry System: (2-oxocyclopent)acetic acid(104115-44-8)

Safety Data

• Hazardous Substances Data: 104115-44-8(Hazardous Substances Data)

Upstream product

• 7647-01-0 hydrogenchloride 
• 41301-66-0 ethyl 1-(2-ethoxy-2-oxoethyl)-2-oxocyclopentanecarboxylate 
• 611-10-9 2-ethoxycarbonyl-1-cyclopentanone 
• 96-32-2 bromoacetic acid methyl ester 
• 141-28-6 diethyl adipate 
• 40702-70-3 ethyl 2-oxo-cyclopentanecarboxylate potassium salt 
• 20826-94-2 ethyl (2-oxocyclopentyl)acetate 
• 844874-18-6 exo-2,3-epoxynorbornane 
• 105-39-5 chloroacetic acid ethyl ester 
• 100796-98-3 {2-[(2,4-Dinitro-phenyl)-hydrazono]-cyclopentyl}-acetic acid 
• 91783-90-3 Cyclopentanon-⁽²⁾-oxalsaeure-⁽¹⁾ 

Downstream Products

• 75066-60-3 3-Oxo-4-(2-oxocyclopentyl)-2-(triphenylphosphoranyliden)butananilid 
• 161779-74-4 (2R,3S,5aS,8aR)-3-Methyl-2-phenyl-hexahydro-1-oxa-3a-aza-cyclopenta[c]pentalen-4-one 
• 161779-70-0 (3R,5aR,8aS)-3-phenyl-hexahydro-1-oxa-3a-aza-cyclopenta[c]pentalen-4-one 
• 1059063-08-9 C₁₄H₁₂ClFN₂O₂ 
• 131348-75-9 (-)-(R)-hexahydro-cyclopenta[b]pyrrol-2-one 
• 1497405-27-2 2-oxycyclopentaneacetic acid benzylamide 
• 1206123-97-8 (R)-2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid, L-arginine salt 
• 1206123-37-6 [(3R)-7-{[4-cyclopentyl-3-(trifluoromethyl)phenyl]methoxy}-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl]acetic acid 
• 1206124-34-6 (R/S)-ethyl 2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetate 
• 206264-62-2 (3S,5aS,8aR)-3-phenyl-hexahydro-1-oxa-3a-aza-cyclopenta[c]pentalen-4-one 
• 1240492-77-6 (3R,5aR,8aS)-3-benzyl-hexahydro-1-oxa-3a-aza-cyclopenta[c]pentalen-4-one 
• 4934-95-6 methyl 2-(2-oxocyclopentyl)acetate 
• 118325-87-4 C₂₃H₃₀O₆S₂ 
• 102472-53-7 (+/-)-cis-1-(toluene-4-sulfonyloxy)-2-[2-(toluene-4-sulfonyloxy)-ethyl]-cyclopentane 

Relevant articles and documents

Acyl acid derivative and preparation method and medical application thereof

The invention relates to an acyl acid derivative as well as a preparation method and medical application thereof. Specifically, the invention relates to a compound represented by a general formula (I), a pharmaceutically acceptable salt thereof, or a pharmaceutical composition containing the same, and the invention also relates to a use thereof as an active ingredient in the prevention and/or treatment of muscle atrophy-related diseases, including myogenic muscle atrophy, disuse muscle atrophy, senile muscle atrophy, neurogenic muscle atrophy, and a use in the prevention and/or treatment of obesity, fatty liver, cardiovascular and cerebrovascular diseases, metabolic diseases, and anti-aging, wherein the definition of each group in the general formula (I) is the same as the definition in the specification.

NOVEL COMPOUNDS

Disclosed are novel retinoid-related orphan receptor gamma (RORγ) modulators and their use in the treatment of diseases mediated by RORγ.

Direct enantioselective bronsted acid catalyzed N-acyliminium cyclization cascades of tryptamines and ketoacids

A direct enantio- and diastereoselective N-acyliminium cyclization cascade through chiral phosphoric acid catalyzed condensation of tryptamines with γ- and δ-ketoacid derivatives to provide architecturally complex heterocycles has been developed. The reac