6305-31-3

Basic information

• Product Name: 1-(4-methylbenzyl)-3-tricyclo[3.3.1.1~3,7~]dec-1-ylurea
• CAS NO: 6305-31-3
• Molecular Formula: C₁₅H₁₃NS
• Molecular Weight: 298.4225
• Mol File: 6305-31-3.mol
• Article Data: 24

Chemical Properties

• Boiling Point: 503.7°C at 760 mmHg
• Flash Point: 178.9°C
• Density: 1.14g/cm³
• Vapor Pressure: 2.83E-10mmHg at 25°C
• Refractive Index: 1.591
• CAS DataBase Reference: 1-(4-methylbenzyl)-3-tricyclo[3.3.1.1~3,7~]dec-1-ylurea(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-methylbenzyl)-3-tricyclo[3.3.1.1~3,7~]dec-1-ylurea(6305-31-3)
• EPA Substance Registry System: 1-(4-methylbenzyl)-3-tricyclo[3.3.1.1~3,7~]dec-1-ylurea(6305-31-3)

Safety Data

• Hazardous Substances Data: 6305-31-3(Hazardous Substances Data)

Usage

General Description

1-(4-methylbenzyl)-3-tricyclo[3.3.1.1~3,7~]dec-1-ylurea is a chemical compound with a complex ring structure and a urea functional group. It is derived from tricyclo[3.3.1.1~3,7~]decane, a bicyclic hydrocarbon with a bridged ring system. The presence of the 4-methylbenzyl group contributes to its aromatic and hydrophobic properties. Ureas are known for their diverse range of applications in organic synthesis, pharmaceuticals, and agrochemicals. The specific properties and potential uses of 1-(4-methylbenzyl)-3-tricyclo[3.3.1.1~3,7~]dec-1-ylurea would depend on its individual chemical and physical characteristics, which would need to be further investigated and characterized.

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Relevant articles and documents

ZnO-NPs catalyzed condensation of 2-aminothiophenol and aryl/alkyl nitriles: Efficient green synthesis of 2-substituted benzothiazoles

The synthesis of 2-substituted benzothiazoles has been described using ZnO-nanoparticles as a catalyst. The condensation of 2-aminothiophenol and aryl/alkyl nitriles resulted in the formation of various 2-substituted benzothiazoles under solvent-free reaction conditions. The library of 2-substituted benzothiazoles has been synthesized in good to excellent yield. The reaction has shown a wide range of functional group compatibility for both varyingly substituted 2-aminothiophenols and nitriles. The protocol has many advantages such as faster reaction rate, mild reaction conditions, various functional group compatibility, excellent yield, solvent-free reaction conditions, easy recovery of materials, and excellent catalyst recyclability, among others. The various advantages of this protocol make it a more feasible, economical, and environmentally benign process.

Ultrasound-assisted efficient and green synthesis of 2-substituted benzothiazoles under solvent-free condition using recyclable sulfated tungstate

Sulfated tungstate catalyzed an efficient and ecofriendly protocol has been described for the synthesis of 2-substituted benzothiazoles. The corresponding benzothiazoles were obtained using a condensation reaction of 2-aminothiophenol with various aldehydes under ultrasound irradiation at room temperature. Various functional groups on the 2-aminothiophenol as well as on the aldehydes were tolerated to provide 2-substituted benzothiazoles derivatives in excellent yields. The faster reaction rate, solvent-free or mild reaction conditions, wide functional group compatibility, excellent yields, easy work-up procedure, and excellent catalyst recyclability are the advantages of this protocol. These advantages make this process more practicable, cost-effective, and environmentally benign.

TBHP/KI-Promoted Annulation of Anilines, Ethers, and Elemental Sulfur: Access to 2-Aryl-, 2-Heteroaryl-, or 2-Alkyl-Substituted Benzothiazoles

An efficient TBHP/KI-promoted annulation of anilines with ethers and elemental sulfur has been developed through the selective C-O bond cleavage of ethers under transition-metal-free conditions. A wide range of 2-aryl-, 2-heteroaryl-, and 2-alkyl-substituted benzothiazoles were easily prepared with satisfactory yields and good functional group compatibility.