88791-03-1

Basic information

• Product Name: Carbamothioic acid, dimethyl-, O-(2-formyl-6-methoxyphenyl) ester
• CAS NO: 88791-03-1
• Molecular Formula: C11H13NO3S
• Molecular Weight: 239.295
• Mol File: 88791-03-1.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Carbamothioic acid, dimethyl-, O-(2-formyl-6-methoxyphenyl) ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamothioic acid, dimethyl-, O-(2-formyl-6-methoxyphenyl) ester(88791-03-1)
• EPA Substance Registry System: Carbamothioic acid, dimethyl-, O-(2-formyl-6-methoxyphenyl) ester(88791-03-1)

Safety Data

• Hazardous Substances Data: 88791-03-1(Hazardous Substances Data)

Upstream product

• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 
• 16420-13-6 N,N-Dimethylthiocarbamoyl chloride 

Downstream Products

• 805246-33-7 2-allylsulfanyl-3-methoxybenzaldehyde 
• 1462267-57-7 (Z)-1-(3-methoxy-2-methylthiophenyl)-2-(3,4,5-trimethoxyphenyl)ethene 
• 1462267-54-4 (E)-3-(3-methoxy-2-methylthiophenyl)-2-(3,4,5-trimethoxyphenyl)prop-2-enoic acid 
• 1312608-59-5 C₄₃H₅₂N₈O₆S 
• 1312610-32-4 C₃₉H₄₆N₆O₄S 
• 1312610-31-3 C₂₇H₃₄B₂O₄S 
• 1312610-30-2 C₁₇H₁₀F₆O₆S₃ 
• 1312610-29-9 C₁₅H₁₂O₂S 
• 1312610-28-8 C₁₇H₁₆O₂S 
• 1312608-58-4 C₄₂H₅₀N₈O₆S 
• 1312610-06-2 C₂₈H₂₈N₆S 
• 1312610-05-1 C₃₈H₄₄N₆O₄S 
• 1312610-04-0 C₂₆H₃₂B₂O₄S 
• 1312610-03-9 C₁₆H₈F₆O₆S₃ 

Relevant articles and documents

Synthesis, crystal structure and conformational analysis of an unexpected [1,5]dithiocine product of aminopyridine and thiovanillin

The condensation reaction of 2-mercapto-3-methoxybenzaldehyde with 3-aminopyridine afforded an unexpected N-alkylated [1,5]dithiocine instead of the N-salicylideneaniline. The proposed mechanism for this condensation involves a strong intramolecular hydro

Divergent Synthesis of Disulfanes and Benzenesulfonothioates Bearing 2-Aminofurans From N-Tosylhydrazone-Bearing Thiocarbamates

An efficient and convenient synthesis of valuable disulfanes and benzenesulfonothioates, having a 2-aminofuran framework, has been developed by employing a copper-catalyzed transformation of readily available N-tosylhydrazone-bearing thiocarbamates. This method features an inexpensive metal catalyst, mild reaction conditions, good functional-group tolerance, short reaction times, and delivers valuable and complex products. A copper carbene generated from an N-tosylhydrazone-bearing thiocarbamate is proposed as the key intermediate for the transformation and it triggers the subsequent cascade. Remarkably, the Ts anion released from N-tosylhydrazone further serves as a nucleophile, thus rendering the formation of benzenesulfonothioates under controlled conditions.

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