7460-90-4

Basic information

• Product Name: 4-[(2-Methyl-2-propenyl)oxy]-1,1'-biphenyl
• Synonyms: 4-[(2-Methyl-2-propenyl)oxy]-1,1'-biphenyl
• CAS NO: 7460-90-4
• Molecular Formula: C₁₆H₁₆O
• Molecular Weight: 0
• Mol File: 7460-90-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 351.6°C at 760 mmHg
• Flash Point: 140°C
• Appearance: /
• Density: 1.005g/cm³
• Vapor Pressure: 8.22E-05mmHg at 25°C
• Refractive Index: 1.549
• CAS DataBase Reference: 4-[(2-Methyl-2-propenyl)oxy]-1,1'-biphenyl(CAS DataBase Reference)
• NIST Chemistry Reference: 4-[(2-Methyl-2-propenyl)oxy]-1,1'-biphenyl(7460-90-4)
• EPA Substance Registry System: 4-[(2-Methyl-2-propenyl)oxy]-1,1'-biphenyl(7460-90-4)

Safety Data

• Hazardous Substances Data: 7460-90-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C16H16O/c1-13(2)12-17-16-10-8-15(9-11-16)14-6-4-3-5-7-14/h3-11H,1,12H2,2H3

Upstream product

• 92-69-3 4-Phenylphenol 
• 563-47-3 3-Chloro-2-methylpropene 

Downstream Products

• 1234845-37-4 (2,2-dimethyl-5-phenyl-2,3-dihydrobenzofuran-7-yl)methanol 
• 1234845-36-3 2,2-dimethyl-5-phenyl-2,3-dihydrobenzofuran-7-carbaldehyde 
• 1234845-35-2 2,2-dimethyl-5-phenyl-2,3-dihydrobenzofuran 
• 107970-02-5 3-Methyl-6-phenyl-2H-chromene 

Relevant articles and documents

GPR120 RECEPTOR AGONISTS AND USES THEREOF

GPR120 agonists are provided. These compounds are useful for the treatment of metabolic diseases, including Type II diabetes and diseases associated with poor glycemic control.

Silanyl phenols and naphthols

There are described silanyl phenols and naphthols of formula (1a) or (1b), wherein R1 is hydrogen; halogen; hydroxy; C1-C20alkyl; C3-C12cycloalkyl; C1-C20alkoxy; trifluoromethyl; pentafluoroethyl; mono- or di-C1-C5alkylamino; hydroxy-C1-C5alkyl; or phenyl, phenyl-C1C20alkyl, phenoxy, phenyl-C1-C20alkoxy, naphthyl or naphthyl-C1-C20alkyl each unsubstituted or substituted by C1-C5alkyl, C3-C12cycloalkyl, C1-C5alkoxy, C3-C12cycloalkoxy, halogen, oxo, carboxy, carboxy-C1-C7alkyl ester, carboxy-C3-C12cycloalkyl ester, cyano, trifluoromethyl, pentafluoroethyl, amino, N,N-mono- or di-C1-C20alkylamino or by nitro; R2, R3 and R4 are each independently of the others hydrogen; C1-C20alkyl; or C3-C12-Cycloalkyl; R5, R6 and R7 are each independently of the others C1-C20alkyl, C5-C10aryl, C1-C20alkoxy, phenyl-C1-C20alkyl, phenyl-C1-C20alkoxy, C2-C5alkenyl, —O—Si—(C1-C5alkyl)3; or O—Si—(C1-C5alkyl)2-O—Si(C1-C5alkyl)3 and n is 0 or 1. The compounds exhibit a pronounced activity against Gram positive and Gram negative bacteria, and also against yeasts and moulds.