503065-08-5

Basic information

• Product Name: Benzaldehyde, 2-(cyclohexylthio)-
• CAS NO: 503065-08-5
• Molecular Formula: C13H16OS
• Molecular Weight: 220.335
• Mol File: 503065-08-5.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 2-(cyclohexylthio)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2-(cyclohexylthio)-(503065-08-5)
• EPA Substance Registry System: Benzaldehyde, 2-(cyclohexylthio)-(503065-08-5)

Safety Data

• Hazardous Substances Data: 503065-08-5(Hazardous Substances Data)

Upstream product

• 1569-69-3 Cyclohexanethiol 
• 552-89-6 2-nitro-benzaldehyde 
• 446-52-6 2-Fluorobenzaldehyde 
• 864512-14-1 2-iodophenyl 4-chlorobenzenesulfonate 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 1174009-26-7 2-(cyclohexylsulfonyl)benzaldehyde 
• 1383611-02-6 (1R,2R)-N,N'-bis(2-(cyclohexylthio)benzylidene)-1,2-cyclohexanediamine 
• 1174009-27-8 2-(3-(2-(cyclohexylsulfonyl)benzyl)-5-fluoro-2-methyl-1H-indol-1-yl)acetic acid ethyl ester 
• 1155694-67-9 2-(3-(2-(cyclohexylsulfonyl)benzyl)-5-fluoro-2-methyl-1H-indol-1-yl)acetic acid 
• 1207539-22-7 (2-(cyclohexylthio)phenyl)methanol 
• 1198110-41-6 5-[2-(cyclohexylsulfanyl)benzylidene]-2,2-dimethyl-1,3-dioxane-4,6-dione 

Relevant articles and documents

Three-Dimensional Heterocycles by Iron-Catalyzed Ring-Closing Sulfoxide Imidation

A general and atom-economical method for the synthesis of cyclic sulfoximines by intramolecular imidations of azido-containing sulfoxides using a commercially available FeII phthalocyanine (FeIIPc) as catalyst has been developed. The method conveys a broad functional group tolerance and the resulting three-dimensional heterocycles can be modified by cross-coupling reactions.

HYDROGENATION OF ESTERS OR CARBONYL GROUPS WITH TETRADENTATE AMINO/IMINO-THIOETHER BASED RUTHENIUM COMPLEXES

The present invention relates to the field of catalytic hydrogenation and, more particularly, to the use of specific ruthenium catalysts, or pre-catalysts, in hydrogenation processes for the reduction of ketones and/or aldehydes into the corresponding alcohol respectively. Said catalysts are ruthenium complexes comprising a tetradentate ligand (L4) coordinating the ruthenium with: two nitrogen atoms, each in the form of a primary or secondary amine (i.e. a NH2 or NH group) or N-alkyl imine functional groups (i.e. a C═N group), and two sulfur atoms, each in the form of thioether functional groups.

Compounds Having CRTH2 Antagonist Activity

Compounds of general formula (I) wherein W is chloro or fluoro; Z is a group SO2R1; wherein R1 is —C3-C8 cycloalkyl or heterocyclyl optionally substituted with one or more substituents chosen from hal