73824-25-6

Basic information

• Product Name: ethyl 2-(1,3-benzoxazol-2-ylsulfanyl)acetate
• Synonyms: ethyl 2-(1,3-benzoxazol-2-ylsulfanyl)acetate
• CAS NO: 73824-25-6
• Molecular Formula: C₁₁H₁₁NO₃S
• Molecular Weight: 237.28
• Mol File: 73824-25-6.mol
• Article Data: 18

Chemical Properties

• Appearance: /
• CAS DataBase Reference: ethyl 2-(1,3-benzoxazol-2-ylsulfanyl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-(1,3-benzoxazol-2-ylsulfanyl)acetate(73824-25-6)
• EPA Substance Registry System: ethyl 2-(1,3-benzoxazol-2-ylsulfanyl)acetate(73824-25-6)

Safety Data

• Hazardous Substances Data: 73824-25-6(Hazardous Substances Data)

Upstream product

• 623-73-4 diazoacetic acid ethyl ester 
• 2382-96-9 2-sulfanyl-1,3-benzoxazole 
• 15091-70-0 2-mercaptobenzoxazole sodium salt 
• 105-39-5 chloroacetic acid ethyl ester 
• 95-55-6 2-amino-phenol 
• 105-36-2 ethyl bromoacetate 

Downstream Products

• 159278-84-9 2-(benzoxazolylthio)acetylhydrazone of p-hydroxybenzaldehyde 
• 1352614-85-7 C₁₈H₁₄ClN₃O₄S 
• 1352614-86-8 C₁₈H₁₃Cl₂N₃O₃S 
• 1352614-87-9 C₁₈H₁₃ClN₄O₅S 
• 1352614-88-0 C₁₈H₁₄ClN₃O₃S 
• 1352614-89-1 C₁₉H₁₆ClN₃O₄S 

Relevant articles and documents

Conjugates with an antimicrobial effect based on new derivatives of mercaptobenzoxazole esterified onto poly(maleic anhydride-alt-vinyl acetate)

New compounds with biological activity based on hydroxy-amino derivatives of benzoxazolyl-2-mercaptoformic acid, benzoxazolyl-2-mercaptoacetic acid, and chloracetyl-2-mercaptobenzoxazole have been synthesized. The chemical bonding of these compounds to po

Preparation method of thioether

The invention relates to a preparation method of thioether, which comprises the following steps: adding mercaptan/phenol and alpha-diazoacetate into an acetonitrile-water mixed solvent, stirring at room temperature under the irradiation of visible light u

Rhodium-Catalyzed Rearrangement of S/Se-Ylides for the Synthesis of Substituted Vinylogous Carbonates

An efficient rhodium-catalyzed unprecedented oxa-[2,3]-sigmatropic rearrangement of sulfur ylide derived from α-thioesters/ketones and diazo carbonyl compounds has been accomplished for the synthesis of various sulfur-tethered vinylogous carbonates in good to excellent yields. Important features of the developed reaction include wide functional group tolerance, excellent chemo- and regioselectivity, and efficient rearrangement involving the carbonyl motif. The present reaction also equally works well with α-selenoesters for the synthesis of seleno-containing vinylogous carbonates.