924-97-0

Basic information

• Product Name: 4-OXOHEPTANOIC ACID
• Synonyms: 4-OXOHEPTANOIC ACID;4-Ketoenanthic acid
• CAS NO: 924-97-0
• Molecular Formula: C₇H₁₂O₃
• Molecular Weight: 144.17
• Mol File: 924-97-0.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 268.7°C at 760 mmHg
• Flash Point: 130.6°C
• Appearance: /
• Density: 1.061g/cm³
• Vapor Pressure: 0.00215mmHg at 25°C
• Refractive Index: 1.443
• CAS DataBase Reference: 4-OXOHEPTANOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-OXOHEPTANOIC ACID(924-97-0)
• EPA Substance Registry System: 4-OXOHEPTANOIC ACID(924-97-0)

Safety Data

• Hazardous Substances Data: 924-97-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H12O3/c1-2-3-6(8)4-5-7(9)10/h2-5H2,1H3,(H,9,10)

Upstream product

• 68245-81-8 2-butyrylsuccinic acid dimethyl ester 
• 17615-01-9 1-(triphenyl-λ⁵-phosphanylidene)pentan-2-one 
• 96-32-2 bromoacetic acid methyl ester 
• 100383-90-2 2-(morpholin-4-yl)pentanenitrile 
• 292638-85-8 acrylic acid methyl ester 
• 201230-82-2 carbon monoxide 
• 557-20-0 diethylzinc 
• 108-30-5 succinic acid anhydride 
• 106-94-5 propyl bromide 
• 137669-41-1 3-Ethoxycarbonyl-3-heptensaeure 
• 3283-25-8 3-Carboxy-3-heptensaeure 
• 30414-54-1 methyl 3-oxohexanoate 
• 141090-16-6 1-ethyl (+/-)-2-ethyl-3-oxohexanedioate 
• 533-68-6 2-bromobutyric acid ethyl ester 

Downstream Products

• 105-21-5 4-propylbutanolide 
• 111-14-8 oenanthic acid 
• 132959-44-5 (-)-(3R,7aS)-3-Phenyl-5-oxo-7a-propyl-2,3,5,6,7,7a-hexahydropyrrolo<2,1-b>oxazole 
• 26524-73-2 5-propylfuran-2(3H)-one 
• 57681-53-5 5-propylfuran-2(5H)-one 
• 120388-32-1 5-propyl-3-(o-chlorobenzyliden)furan-2-one 
• 1174409-44-9 C₁₄H₂₅NO₂ 
• 1427215-16-4 2-(1-(4-chlorobenzoyl)-5-methoxy-2-propyl-1H-indol-3-yl)acetic acid 
• 1427215-01-7 C₂₁H₂₀ClNO₄ 
• 22094-43-5 4-Hydroxy-heptansaeure-hydrazid 
• 77919-72-3 C₂₂H₂₆N₄O₂S 
• 77919-68-7 C₂₀H₂₁ClN₄OS 
• 77919-77-8 4-(4-Ethoxy-phenyl)-5-(2-propyl-1H-indol-3-ylmethyl)-4H-[1,2,4]triazole-3-thiol 
• 77919-69-8 C₂₁H₂₄N₄OS 

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.

SUBSTITUTED AMINO-BENZIMIDAZOLES, MEDICAMENTS COMPRISING SAID COMPOUND, THEIR USE AND THEIR METHOD OF MANUFACTURE

The present invention relates to substituted amino-benzimidazoles of general formula (1) wherein the groups R1 to R14 and A, are defined as in the specification and claims and the use thereof for the treatment of Alzheimer's disease (AD) and similar diseases.

Method for preparing chiral diphosphines

The invention concerns a method for preparing a compound of formula (1) wherein: A represents naphthyl or phenyl optionally substituted; and Ar1, Ar2independently represent a saturated or aromatic carbocyclic group, optionally substituted.