1262322-65-5

Basic information

• Product Name: C₁₈H₁₇NO₃S
• Synonyms: C₁₈H₁₇NO₃S
• CAS NO: 1262322-65-5
• Molecular Weight: 327.404
• Mol File: 1262322-65-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: C₁₈H₁₇NO₃S(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₈H₁₇NO₃S(1262322-65-5)
• EPA Substance Registry System: C₁₈H₁₇NO₃S(1262322-65-5)

Safety Data

• Hazardous Substances Data: 1262322-65-5(Hazardous Substances Data)

Upstream product

• 65127-52-8 1-(4-methyl-1H-indol-3-yl)ethan-1-one 
• 98-59-9 p-toluenesulfonyl chloride 
• 858101-82-3 4-methyl-1-tosyl-1H-indole-3-carbaldehyde 
• 4771-48-6 4-methyl-1H-indole-3-carboxaldehyde 
• 16096-32-5 4-methyl-1H-indole 
• 112970-65-7 4-methyl-1-tosyl-1H-indole 
• 108-24-7 acetic anhydride 

Downstream Products

• 1262322-54-2 C₁₉H₂₁N₅O₂S 

Relevant articles and documents

A radical addition and cyclization relay promoted by Mn(OAc)3?2H2O: Synthesis of 1,2-oxaphospholoindoles and mechanistic study

Novel and efficient Mn(OAc)3?2H2O promoted radical addition-[4 + 1] cyclization relay of 3-indolymethanols and phosphites was disclosed, which afforded 1,2-oxaphospholoindole derivatives in moderate to good yields. Based on the experimental and computational studies, a mechanism involving radical addition and intramolecular cyclization cascade was proposed.

Antifungal agents. Part 3: Synthesis and antifungal activities of 3-acylindole analogs against phytopathogenic fungi in vitro

To find more potent antifungal compounds, twenty 3-acylindole analogs were synthesized and bio-evaluated for their antifungal activities against seven phytopathogenic fungi. Structure-activity relationships investigations revealed that 4- or 6-methyl and 3-acetyl or propionyl groups were the important structural properties of 3-acylindoles for the activities. Especially 4-methyl-3-propionylindole, 12, displayed the more potent activities than hymexazol, a commercially available agricultural fungicide, and might be considered as a new promising lead candidate for further design and synthesis of agricultural fungicides.