53606-33-0

Basic information

• Product Name: Benzaldehyde, 2-(ethylthio)-
• Synonyms: 2-(ethylthio)benzaldehyde;Benzaldehyde,2-(ethylthio);o-ethylmercapto-benzaldehyde;2-(ethylsulfanyl)benzenecarbaldehyde
• CAS NO: 53606-33-0
• Molecular Formula: C9H10OS
• Molecular Weight: 166.244
• Mol File: 53606-33-0.mol
• Article Data: 16

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 2-(ethylthio)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2-(ethylthio)-(53606-33-0)
• EPA Substance Registry System: Benzaldehyde, 2-(ethylthio)-(53606-33-0)

Safety Data

• Hazardous Substances Data: 53606-33-0(Hazardous Substances Data)

Upstream product

• 37527-69-8 (2-ethylsulfanyl-phenyl)-methanol 
• 68-12-2 N,N-dimethyl-formamide 
• 6630-33-7 ortho-bromobenzaldehyde 
• 75-08-1 ethanethiol 
• 89-98-5 2-chloro-benzaldehyde 
• 446-52-6 2-Fluorobenzaldehyde 
• 811-51-8 sodium thioethylate 
• 4521-31-7 o-hydroxymethyl thiophenol 
• 60-24-2 2-hydroxyethanethiol 

Downstream Products

• 900175-31-7 (E)-ethyl 4-(2-(ethylthio)benzylideneamino)butanoate 
• 900175-36-2 (2R,3S)-ethyl 2-(2-(ethylsulfonyl)phenyl)pyrrolidine-3-carboxylate 
• 22720-75-8 2-acetyl benzo[b]thiophene 
• 330944-87-1 2-[2'-(ethylsulfonyl)-4'-nitrobenzyl]pyridine 

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.

SULFUR CHELATED RUTHENIUM COMPOUNDS USEFUL AS OLEFIN METATHESIS CATALYSTS

Sulfur chelated ruthenium compounds represented by the following formula: wherein M indicates the ruthenium metal bound to a benzylidene carbon; R represents C1-C7 alkyl group or optionally substituted aryl; X1 and X2 each independently represent halogen; Y1 and Y2 each independently denote unsubstituted or alkyl-substituted phenyl; and Z independently represents hydrogen, electron withdrawing or electron donating substituent, with m being an integer from 1 to 4, and processes and compositions related thereto.

New CRTH2 Antagonists

The present invention relates to a compound of formula (I), to the process for preparing such compounds and to their use in the treatment of a pathological condition or disease susceptible to amelioration by CRTh2 antagonist activity.