37527-69-8

Basic information

• Product Name: Benzenemethanol, 2-(ethylthio)-
• CAS NO: 37527-69-8
• Molecular Formula: C9H12OS
• Molecular Weight: 168.26
• Mol File: 37527-69-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 2-(ethylthio)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 2-(ethylthio)-(37527-69-8)
• EPA Substance Registry System: Benzenemethanol, 2-(ethylthio)-(37527-69-8)

Safety Data

• Hazardous Substances Data: 37527-69-8(Hazardous Substances Data)

Upstream product

• 21101-79-1 2-ethylsulfanylbenzoic acid 
• 53606-33-0 2-(ethylsulfanyl)benzenecarbaldehyde 
• 6630-33-7 ortho-bromobenzaldehyde 
• 4892-02-8 Methyl thiosalicylate 
• 3795-78-6 2-ethylsulfanyl-benzoic acid methyl ester 
• 4521-31-7 o-hydroxymethyl thiophenol 
• 75-03-6 ethyl iodide 

Downstream Products

• 23121-10-0 1-chloromethyl-2-ethanesulfonyl-benzene 
• 1352128-46-1 8-(2-ethanesulfonyl-benzyl)-2-methylsulfanyl-8H-pyrido[2,3-d]-pyrimidin-7-one 
• 1352128-14-3 8-(2-ethanesulfonyl-benzyl)-2-[4-(4-methyl-piperazin-1-yl)-phenylamino]-8H-pyrido[2,3-d]pyrimidin-7-one 
• 1352128-48-3 6-bromo-8-(2-ethanesulfonyl-benzyl)-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-one 
• 1352128-49-4 6-bromo-8-(2-ethanesulfonylbenzyl)-2-methanesulfinyl-8H-pyrido[2,3-d]pyrimidin-7-one 
• 1352128-50-7 6-bromo-8-(2-ethanesulfonylbenzyl)-2-[4-(4-methyl-piperazin-1-yl)-phenylamino]-8H-pyrido[2,3-d]pyrimidin-7-one 
• 1352128-17-6 8-(2-ethanesulfonylbenzyl)-2-[4-(4-methyl-piperazin-1-yl)-phenylamino]-6-phenyl-8H-pyrido[2,3-d]pyrimidin-7-one 
• 37527-74-5 2-Ethylthiophenylessigsaeure 
• 37527-72-3 2-Ethylthiobenzylcyanid 
• 37527-76-7 (2-ethylsulfanyl-phenyl)-acetic acid methyl ester 
• 37527-80-3 (2-Ethanesulfinyl-phenyl)-acetic acid methyl ester 
• 498534-34-2 2-(2'-ethylsulfonylbenzyl)-1,10-phenanthroline 
• 498534-32-0 2-(2'-ethylthiobenzyl)-1,10-phenanthroline 
• 498534-36-4 (2-ethylthio)benzyl bromide 

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.

8-(SULFONYLBENZYL)PYRIDO[2,3-D]PYRIMIDIN-7(8H)-ONES FOR THE TREATMENT OF CNS DISORDERS

Provided herein are PAK inhibitors and methods of utilizing PAK inhibitors for the treatment of CNS disorders.

Pyrazinone thrombin inhibitors

Compounds of the invention are useful in inhibiting thrombin and associated thrombotic occlusions having the following structure: or a pharmaceutically acceptable salt thereof, wherein A is