18859-38-6

Basic information

• Product Name: AURORA 17222
• Synonyms: AURORA 17222;CHEMBRDG-BB 6976862;OTAVA-BB BB7013070009;1-(BIPHENYL-4-YLOXY)ACETONE;AKOS BBS-00008911;OTAVA-BB 7013070009;1-(biphenyl-4-yloxy)acetone(SALTDATA: FREE);1-([1,1′-Biphenyl]-4-yloxy)acetone
• CAS NO: 18859-38-6
• Molecular Formula: C₁₅H₁₄O₂
• Molecular Weight: 226.27
• Mol File: 18859-38-6.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 369 °C at 760 mmHg
• Flash Point: 165.9 °C
• Appearance: /
• Density: 1.083 g/cm³
• Vapor Pressure: 1.22E-05mmHg at 25°C
• Refractive Index: 1.552
• CAS DataBase Reference: AURORA 17222(CAS DataBase Reference)
• NIST Chemistry Reference: AURORA 17222(18859-38-6)
• EPA Substance Registry System: AURORA 17222(18859-38-6)

Safety Data

• Hazard Codes: N
• Statements: 50
• Safety Statements: 61
• Hazardous Substances Data: 18859-38-6(Hazardous Substances Data)

Usage

General Description

AURORA 17222 is a chemical compound that consists of a mixture of various chemicals, including aluminum oxide, barium sulfate, and iron oxide. It is commonly used as a pigment in the production of paints, coatings, and plastics. AURORA 17222 is known for its high quality and durability, making it a popular choice for industrial and commercial applications. It is also used in the manufacturing of automotive and aerospace components, where a long-lasting and weather-resistant finish is required. Additionally, AURORA 17222 is often used in the formulation of specialty inks and dyes for printing and textile industries, providing vibrant and fade-resistant colors. Overall, AURORA 17222 is a versatile and reliable chemical compound with a wide range of industrial uses.

InChI:InChI=1/C15H14O2/c1-12(16)11-17-15-9-7-14(8-10-15)13-5-3-2-4-6-13/h2-10H,11H2,1H3

Upstream product

• 92-69-3 4-Phenylphenol 
• 78-95-5 chloroacetone 
• 2684-62-0 diazoacetone 
• 75-56-9 methyloxirane 

Downstream Products

• 5333-65-3 1-(Biphenyl-4-yloxy)-propan-2-ol 

Relevant articles and documents

Iridium-catalyzed enantioselective intramolecular hydroarylation of allylic aryl ethers devoid of a directing group on the aryl group

Although intramolecular hydroarylation is an attractive transformation of allylic aryl ethers, it has suffered from narrow substrate scope. We herein describe Ir/(S)-DTBM-SEGPHOS-catalyzed intramolecular hydroarylation of allylic aryl ethers. The reaction

DIPHENYLOXYALKYLAMINE DERIVATIVES AND ARYLOXYALKYLAMINE DERIVATIVES, PHARMACEUTICAL COMPOSITION, USE OF SAID PHARMACEUTICAL COMPOSITION FOR TREATING, PREVENTING OR INHIBITING CHRONIC PULMONARY INFLAMMATORY DISEASES AND METHOD FOR TREATING OR PREVENTING SU

The present invention relates to diphenyloxyalkylamine derivatives and aryloxyalkylamine derivatives that are structurally analogous to mexiletine, said derivatives having important biological activity and not causing the undesired side effects observed w

Formation of ketones from alkyl nitrites in the solid state

Alkyl nitrites selectively afforded the corresponding ketones upon photoirradiation in the solid state. It was suggested by the X-ray crystallographic analysis that the cavity in crystal and the initial conformation of the nitroso group had an influence on the yield of the ketones.