57502-57-5

Basic information

• Product Name: (Z)-1-tosyl-2,3,6,7-tetrahydro-1H-azepine
• Synonyms: (Z)-1-tosyl-2,3,6,7-tetrahydro-1H-azepine;1-Tosyl-2,3,6,7-tetrahydro-1H-azepine;1-(4-methylphenyl)sulfonyl-2,3,6,7-tetrahydroazepine
• CAS NO: 57502-57-5
• Molecular Formula: C₁₃H₁₇NO₂S
• Molecular Weight: 251.34458
• Mol File: 57502-57-5.mol
• Article Data: 54

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (Z)-1-tosyl-2,3,6,7-tetrahydro-1H-azepine(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-1-tosyl-2,3,6,7-tetrahydro-1H-azepine(57502-57-5)
• EPA Substance Registry System: (Z)-1-tosyl-2,3,6,7-tetrahydro-1H-azepine(57502-57-5)

Safety Data

• Hazardous Substances Data: 57502-57-5(Hazardous Substances Data)

Usage

General Description

(Z)-1-tosyl-2,3,6,7-tetrahydro-1H-azepine is a chemical compound with the molecular formula C15H21NO2S. It is a tosylated derivative of azepine, a seven-membered heterocyclic compound containing a nitrogen atom in the ring. (Z)-1-tosyl-2,3,6,7-tetrahydro-1H-azepine is a potentially useful building block in organic synthesis, particularly in the synthesis of complex natural products or pharmaceutical compounds. It may also have biological activity or therapeutic potential, although specific applications or effects are not widely documented. The tosyl group, a functional group consisting of a tosylate ion attached to a benzene ring, can serve as a protecting group in some reactions or as a precursor for further functionalization of the molecule. Overall, (Z)-1-tosyl-2,3,6,7-tetrahydro-1H-azepine is a versatile and potentially valuable compound in the field of organic chemistry.

Upstream product

• 104144-06-1 N,N-di-3-butenyl-p-toluenesulfonamide 
• 176729-83-2 N-allyl-4-methyl-N-(pent-4-en-1-yl)benzenesulfonamide 
• 70-55-3 toluene-4-sulfonamide 

Downstream Products

• 1004763-14-7 2-{4-[3-(2-methylpyrrolidin-1-yl)propoxy]phenyl}-5,6,7,8-tetrahydro-4H-[1,3]thiazolo[4,5-d]azepine 
• 1334179-67-7 C₂₈H₃₅N₃O₃S₂ 
• 1334179-66-6 5-bromo-1-tosylazepan-4-one 
• 1334179-65-5 C₁₃H₁₈BrNO₃S 

Relevant articles and documents

Advanced fine-tuning of grubbs/hoveyda olefin metathesis catalysts: A further step toward an optimum balance between antinomic properties

A 95% yield in the cross metathesis of acrylonitrile with a model olefin is achieved at 25 °C with only 3 mol % of the new air-stable ruthenium catalyst 1f shown in the enclosed structural diagram. Even more remarkable are the performances of its boosted

Protection of Ruthenium Olefin Metathesis Catalysts by Encapsulation in a Self-assembled Resorcinarene Capsule

Catalyst encapsulation is examined as a means of increasing the productivity of olefin metathesis catalysts. Commercially available, cationic ruthenium metathesis catalysts were incorporated into a supramolecular resorcin[4]arene capsule. Encapsulation increased catalyst stability in water-saturated toluene, delivering higher metathesis yields than the parent, non-encapsulated Hoveyda catalyst in the same reaction medium.

Visible-Light-Controlled Ruthenium-Catalyzed Olefin Metathesis

Olefin metathesis is now one of the most efficient ways to create new carbon-carbon bonds. While most efforts focused on the development of ever-more efficient catalysts, a particular attention has recently been devoted to developing latent metathesis cat

Nitrogen-coordination-containing ruthenium carbene catalyst and preparation method and application thereof

The present invention discloses a nitrogen-coordination-containing ruthenium carbene catalyst and a preparation method and application thereof. The nitrogen-coordination-containing ruthenium carbene catalyst is characterized by being shown in a formula (I