7600-00-2

Basic information

• Product Name: 2-Cyclohexen-1-one, 2,2'-(phenylmethylene)bis[3-hydroxy-5,5-dimethyl-
• CAS NO: 7600-00-2
• Molecular Formula: C23H28O4
• Molecular Weight: 368.473
• Mol File: 7600-00-2.mol
• Article Data: 83

Chemical Properties

• CAS DataBase Reference: 2-Cyclohexen-1-one, 2,2'-(phenylmethylene)bis[3-hydroxy-5,5-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclohexen-1-one, 2,2'-(phenylmethylene)bis[3-hydroxy-5,5-dimethyl-(7600-00-2)
• EPA Substance Registry System: 2-Cyclohexen-1-one, 2,2'-(phenylmethylene)bis[3-hydroxy-5,5-dimethyl-(7600-00-2)

Safety Data

• Hazardous Substances Data: 7600-00-2(Hazardous Substances Data)

Upstream product

• 348-54-9 2-Fluoroaniline 
• 100-52-7 benzaldehyde 
• 126-81-8 dimedone 
• 62-53-3 aniline 
• 1445-69-8 2,3-dihydrophthalazine-1,4-dione 
• 3471-13-4 dimedone 
• 7605-28-9 2-(phenylsulfonyl)acetonitrile 
• 1666-17-7 benzaldehyde p-toluenesulfonylhydrazone 
• 135-19-3 β-naphthol 
• 108-48-5 2,6-dimethylpyridine 
• 105-56-6 ethyl 2-cyanoacetate 
• 3376-23-6 N-methyl-α-phenylnitrone 
• 105-45-3 acetoacetic acid methyl ester 
• 100-39-0 benzyl bromide 

Downstream Products

• 19744-83-3 3,3,6,6-tetramethyl-9-phenyl-3,4,5,6,7,9-hexahydro-1H-xanthene-1,8-(2H)-dione 
• 37587-36-3 3,3-dimethyl-11-phenyl-2,3,4,5,10,11-hexahydro-1H-dibenzo<1,4>diazepin-1-one 
• 868992-00-1 10-hydroxy-3,3,6,6-tetramethyl-9-phenyl-1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-dione 
• 1448188-75-7 2,2'-(1-phenylethane-1,1-diyl)bis(3-hydroxy-5,5-dimethylcyclohex-2-enone) 
• 13337-64-9 ethyl 1,4,7,8-tetrahydro-2,7,7-trimethyl-4-phenyl-5(6H)-oxoquinoline-3-carboxylate 
• 19997-22-9 spiro[(6,6-dimethyl-4-oxo-3-phenyl-2,3,4,5,6,7-hexahydrobenzofuran)-2,2'-(5,5-dimethylcyclohexane-1,3-dione)] 
• 118966-46-4 4',4',6,6-tetramethyl-2-phenyl-6,7-dihydro-2H-spiro[benzofuran-3,1'-cyclohexane]-2',4,6'(5H)-trione 

Relevant articles and documents

Facile Synthesis of Azaarene-Substituted Hydroxycoumarins Possessing High Biological Activities via Three-Component C(sp3)-H Functionalization

An unprecedented three-component C(sp3)-H functionalization of 2-alkylazaarenes with aryl aldehydes and 4-hydroxycoumarins was realized, providing azaarene-substituted 3-benzyl-4-hydroxycoumarins in good to excellent yields. These new target compounds displayed broad-spectrum antibacterial activities, providing a new type of antibacterial skeleton.

One-pot two-step mechanochemical synthesis of arylsulfonyl 4H-pyrans

In this paper, a simple and environment-friendly protocol was developed for the synthesis of arylsulfonyl 4H-pyrans via L-proline-catalyzed one-pot two-step reaction of aromatic aldehyde with phenylsulphonyl acetonitrile and dimedone under ball-milling conditions. Environmental acceptability, wide substrate scope, low cost and operational simplicity are the key features of this method.

Montmorillonite KSF-Catalyzed Synthesis of 2,2′-(Arylmethylene)bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-ones) for the Functionalization of MCM-41 Silica Nanoparticles

Abstract: A green protocol has been developed for the preparation of 2,2′-(arylmethylene)bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-ones) following the multicomponent condensation reaction between aromatic alde-hydes and dimedone with excellent yields. The

On the enantioselective phosphoric-acid-catalyzed hantzsch synthesis of polyhydroquinolines

A reinvestigation of a chiral phosphoric-acid-catalyzed four-component Hantzsch enantioselective synthesis of polyhydroquinolines reported in 2009 is presented. In our hands, when the reaction was performed with fidelity to the original report using a chiral enantiopure phosphoric acid catalyst, no enantioselectivity was observed. Unlike in the original report, enantioselectivity results are backed by baseline separation of the enantiomers by HPLC analyses on chiral stationary phase with UV and chiroptical detection.