60315-73-3

Basic information

• Product Name: 4-chloro-2-formylphenyl acetate
• CAS NO: 60315-73-3
• Molecular Formula: C₉H₇ClO₃
• Molecular Weight: 198.6031
• Mol File: 60315-73-3.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 303°C at 760 mmHg
• Flash Point: 133.7°C
• Density: 1.318g/cm³
• Vapor Pressure: 0.000958mmHg at 25°C
• Refractive Index: 1.567
• CAS DataBase Reference: 4-chloro-2-formylphenyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-chloro-2-formylphenyl acetate(60315-73-3)
• EPA Substance Registry System: 4-chloro-2-formylphenyl acetate(60315-73-3)

Safety Data

• Hazardous Substances Data: 60315-73-3(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 635-93-8 5-chlorosalicyclaldehyde 

Downstream Products

• 109165-17-5 5-chloro-2-hydroxybenzaldehyde dimethyl acetal 
• 635-93-8 5-chlorosalicyclaldehyde 
• 127890-30-6 Acetic acid (5-chloro-2-hydroxy-phenyl)-(dimethoxy-phosphoryl)-methyl ester 
• 1362456-22-1 2-(3-acetyl-5-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-2,3-dihydro-1,3,4-oxadiazol-2-yl)-4-chlorophenyl acetate 
• 1362456-32-3 C₁₈H₁₅ClN₂O₅ 
• 332131-26-7 C₉H₉ClO₃ 

Relevant articles and documents

INHIBITORS OF GLUCOSE TRANSPORTERS (GLUTS)

The present invention relates to 2,6-methanobenzo[g][1]oxacin-4-onecompounds and their analog compounds and pharmaceutically acceptable salts thereof as selective inhibitor of glucose transporters 1 and 3 (GLUTs 1 and 3), to methods of preparing said compounds, and to the use thereof as pharmaceutically active agents, especially for the prophylaxis and/or treatment of metabolic diseases, immunological diseases, autoimmune diseases, inflammation, graft versus host disease, cancer, and metastasis thereof. Furthermore, the present invention is directed to pharmaceutical composition comprising at least one of 2,6-methanobenzo[g][1]oxacin-4-one compounds and their analog compounds.

A mild and efficient acetylation of alcohols, phenols and amines with acetic anhydride using La(NO3)3·6H2O as a catalyst under solvent-free conditions

A wide variety of alcohols, phenols and amines are efficiently and selectively converted into the corresponding acetates by treatment with acetic anhydride in the presence of catalytic amounts of La(NO3)3·6H2O under solvent-free conditions at room temperature. The method is compatible with acid sensitive hydroxyl protecting groups such as TBDMS, THP, OBz, OBn, Boc and some isopropylidenes and offers excellent yields of the mono acetates of 1,3-, 1,4- and 1,5-diols.