36056-09-4

Basic information

• Product Name: Benzene, [(1-ethoxyethyl)thio]-
• CAS NO: 36056-09-4
• Molecular Formula: C10H14OS
• Molecular Weight: 182.287
• Mol File: 36056-09-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzene, [(1-ethoxyethyl)thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [(1-ethoxyethyl)thio]-(36056-09-4)
• EPA Substance Registry System: Benzene, [(1-ethoxyethyl)thio]-(36056-09-4)

Safety Data

• Hazardous Substances Data: 36056-09-4(Hazardous Substances Data)

Upstream product

• 60-29-7 diethyl ether 
• 882-33-7 diphenyldisulfane 
• 108-98-5 thiophenol 
• 109-92-2 ethyl vinyl ether 
• 926-67-0 O-Ethyl thioacetate 
• 981-18-0 triphenyl(phenylazo)methane 

Downstream Products

• 90449-89-1 2-(1-ethoxyethyl)-1-cyclopentanone 
• 71369-95-4 2-(1-phenylthioethyl)cyclohexanone 
• 90449-84-6 2-(1'-ethoxyethyl)-1-cyclohexanone 
• 36195-58-1 (E)-1-phenyl-3-phenylthio-1-butene 
• 23785-44-6 3-Ethoxy-thiobutyric acid S-phenyl ester 

Relevant articles and documents

Visible-Light-Induced Direct Thiolation at α-C(sp3)-H of Ethers with Disulfides Using Acridine Red as Photocatalyst

A simple and efficient method for the preparation of α-arylthioethers through a visible-light-induced direct thiolation at α-C(sp3)-H of ethers with diaryl disulfides was developed using acridine red as a novel photocatalyst. The reactions occurred at ambient conditions and generated the corresponding products in good to excellent yields, ignoring steric effect of disulfides.

Synthesis of dithioacetals and oxathioacetals with chiral auxiliaries

One-pot synthesis of dithioacetals as well as an efficient method for oxathioacetal is reported. Additionally, some chiral auxiliaries were used to synthesize enantiomerically pure dithioacetals and oxathioacetals.

REACTION OF THIONOCARBOXYLATE ESTERS WITH PHENYLAZOTRIPHENYLMETHANE

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