35288-13-2

Basic information

• Product Name: 4-cyclohexyl-gamma-oxobenzenebutyric acid
• Synonyms: 4-cyclohexyl-gamma-oxobenzenebutyric acid;4-Cyclohexyl-α-oxobenzenebutanoic acid;4-CYCLOHEXYL-GAMMA-OXOBENZENEBUTYRIC ACID(WXC07262)
• CAS NO: 35288-13-2
• Molecular Formula: C₁₆H₂₀O₃
• Molecular Weight: 260.3282
• EINECS: 252-489-7
• Mol File: 35288-13-2.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 462.9 °C at 760 mmHg
• Flash Point: 247.9 °C
• Appearance: /
• Density: 1.132 g/cm³
• CAS DataBase Reference: 4-cyclohexyl-gamma-oxobenzenebutyric acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-cyclohexyl-gamma-oxobenzenebutyric acid(35288-13-2)
• EPA Substance Registry System: 4-cyclohexyl-gamma-oxobenzenebutyric acid(35288-13-2)

Safety Data

• Hazardous Substances Data: 35288-13-2(Hazardous Substances Data)

Upstream product

• 108-30-5 succinic acid anhydride 
• 827-52-1 1-phenyl-1-cyclohexane 
• 7446-70-0 aluminium trichloride 
• 98-95-3 nitrobenzene 
• 115199-59-2 ethyl 4-(p-cyclohexylphenyl)-4-oxobutanoate 
• 58897-74-8 (E)-4-(4-cyclohexylphenyl)-4-oxobut-2-enoic acid 
• 110-83-8 cyclohexene 

Downstream Products

• 51036-98-7 3-(3,4-dimethylbenzoyl)propionic acid 
• 35288-08-5 4-(4-tert-butylphenyl)-4-oxobutyric acid 
• 75382-32-0 3-(5-indanylcarbonyl)-propionic acid 
• 115199-59-2 ethyl 4-(p-cyclohexylphenyl)-4-oxobutanoate 
• 32808-55-2 4-(4-cyclohexyl-3-nitrophenyl)-4-oxobutyric acid 
• 36330-85-5 3-(p-phenyl)benzoylpropionic acid 
• 56462-19-2 4-(4-cyclohexyl-phenyl)-butyryl chloride 
• 64959-04-2 7-cyclohexyl-3,4-dihydro-1(2H)-naphthalenone 
• 93151-09-8 6-cyclohexyltetralin 
• 97728-49-9 dimethyl 2-(4-cyclohexylphenyl)succinate 
• 97798-05-5 5-(4-cyclohexylphenyl)furan-2(3H)-one 
• 54338-32-8 4-(4-cyclohexylphenyl)butanoic Acid 

Relevant articles and documents

4-Imidazole derivatives of benzyl and restricted benzyl sulfonamides, sulfamides, ureas, carbamates, and amides and their use

Compounds of formula I are useful in treating diseases prevented by or ameliorated with α1A agonists. Also disclosed are α1A agonist compositions and a method of activating α1 adrenoceptors in a mammal.

Phosphonic acid compounds, their production and use

The present invention relates to a compound of the general formula (I): STR1 wherein ring A is a benzene ring that may be substituted; Y is a divalent group as a constituent member of ring B forming a 5- to 8-membered ring; Q1 is a group of the formula --X--P(O)(OR1)(OR2) wherein X is a bond or a divalent group; R1 and R2, identical or different, are hydrogen or a lower alkyl, or may be combined together to form a ring; Q2 is hydrogen, a hydrocarbon group that may be substituted or a heterocyclic group that may be substituted; and the group of the formula --CON(Q1)(Q2) is connected to the a- or b-position carbon atom, or a salt thereof, which is useful as prophylactic and therapeutic agents of various metabolic bone diseases such as osteoporosis.

Oxidative 1,2-aryl migration of alkyl aryl ketones by using diacetoxyphenyliodine: Synthesis of arylacetate, 2-arylpropanoate, and 2-arylsuccinate

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