84589-30-0

Basic information

• Product Name: 2-(1,3-benzoxazol-2-ylsulfanyl)-1-phenylethanone
• Synonyms: 2-(1,3-benzoxazol-2-ylsulfanyl)-1-phenylethanone
• CAS NO: 84589-30-0
• Molecular Formula: C₁₅H₁₁NO₂S
• Molecular Weight: 269.31834
• Mol File: 84589-30-0.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(1,3-benzoxazol-2-ylsulfanyl)-1-phenylethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(1,3-benzoxazol-2-ylsulfanyl)-1-phenylethanone(84589-30-0)
• EPA Substance Registry System: 2-(1,3-benzoxazol-2-ylsulfanyl)-1-phenylethanone(84589-30-0)

Safety Data

• Hazardous Substances Data: 84589-30-0(Hazardous Substances Data)

Upstream product

• 2382-96-9 benzo[d]oxazole-2-(3H)-thione 
• 532-27-4 1-chloroacetophenone 
• 15091-70-0 2-mercaptobenzoxazole sodium salt 
• 70-11-1 α-bromoacetophenone 
• 2382-96-9 2-sulfanyl-1,3-benzoxazole 
• 98-86-2 acetophenone 

Downstream Products

• 3394-24-9 2-(2-hydroxyphenylamino)-4-phenylthiazole 
• 84589-32-2 2-(2-hydroxyphenylimino)-5-phenyl-1,3,4-thiadiazine 
• 84589-34-4 3-methyl-4-(4-phenhylthiazol-2-yl)-4H-1,4-benzoxazine 
• 1498-99-3 styrenesulfide 
• 1241899-67-1 2-(benzo[d]oxazol-2-ylsulfonyl)-1-phenylethanone 

Relevant articles and documents

In vitro anti-Candida activity and action mode of benzoxazole derivatives

A newly synthetized series of N-phenacyl derivatives of 2-mercaptobenzoxazole, including analogues of 5-bromo- and 5,7-dibromobenzoxazole, were screened against Candida strains and the action mechanism was evaluated. 2-(1,3-benzoxazol-2-ylsulfanyl)-1-(4-b

KI/K 2 S 2 O 8 -Mediated α-C-H Sulfenylation of Carbonyl Compounds with (Hetero)Aryl Thiols

A new and facile KI/K 2 S 2 O 8 -mediated α-C-H sulfenylation of carbonyl compounds with (hetero)aryl thiols was developed for the formation of C-S bond at room temperature. This method provided a simple process for the sy

Synthesis of α-sulfenyl monoketones: Via a metal-free oxidative cross dehydrogenative coupling (CDC) reaction

α-Sulfenyl ketones are potential precursors which find a variety of applications in organic synthesis. Their typical synthesis requires pre-functionalized starting materials and two to three step synthetic sequences. In addition, the selective pre-functionalization of unsymmetrical ketones is a challenge, which limits the synthesis of the desired sulfenylated ketones. To overcome these disadvantages, a metal-free, convenient one-step strategy for synthesizing α-sulfenyl ketones at ambient temperature via a cross-dehydrogenative coupling (CDC) strategy has been developed with a broad substrate scope. Therefore, this CDC strategy for C-S bond formation is attractive and may find wide applications in organic synthesis.