1092461-45-4

Basic information

• Product Name: N-[(3R)-3-(4-methoxyphenyl)pentanoyl]bornane-10,2-sultam
• Synonyms: N-[(3R)-3-(4-methoxyphenyl)pentanoyl]bornane-10,2-sultam
• CAS NO: 1092461-45-4
• Molecular Weight: 405.558
• Mol File: 1092461-45-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-[(3R)-3-(4-methoxyphenyl)pentanoyl]bornane-10,2-sultam(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(3R)-3-(4-methoxyphenyl)pentanoyl]bornane-10,2-sultam(1092461-45-4)
• EPA Substance Registry System: N-[(3R)-3-(4-methoxyphenyl)pentanoyl]bornane-10,2-sultam(1092461-45-4)

Safety Data

• Hazardous Substances Data: 1092461-45-4(Hazardous Substances Data)

Upstream product

• 925-90-6 ethylmagnesium bromide 
• 34446-64-5 (E)-3-(4-methoxyphenyl)propenoyl chloride 
• 153141-25-4 (1S)-N-(p-methoxycinamoyl)-2,10-camphorsultam 
• 94594-90-8 (2R)-bornane-10,2-sultam 

Downstream Products

• 824984-24-9 (3R)-3-(4-methoxyphenyl)pentan-1-ol 

Relevant articles and documents

Grignard 1,4-Additions to para-Substituted (2R)-N-Cinnamoylbornane-10,2-sultam Derivatives: Revised Configuration for the N,OAc-Keteneacetal Formation in the Presence of Cu(I)

Using a19F-NMR analytical method, we have corrected and improved the linear correlation initially found between the diastereoselectivity observed during the EtMgBr conjugated addition to Michael acceptors of type 1, as a function of their σsub

Chiral γ-aryl-1H-1,2,4-triazole derivatives as highly potential antifungal agents: Design, synthesis, structure, and in vitro fungicidal activities

A novel series of chiral γ-aryl-1H-1,2,4-triazole derivatives as highly potential antifungal agents have been designed and synthesized conveniently by using the chiral auxiliary as a controlling reagent. All of the compounds exhibit moderate to high ee va