59883-07-7

Basic information

• Product Name: RUBIDATE UV
• Synonyms: RUBIDATE UV;Diethyl 1,4-dihydroxynaphthalene-2,3-dicarboxylate
• CAS NO: 59883-07-7
• Molecular Formula: C₁₆H₁₆O₆
• Molecular Weight: 304.296
• Mol File: 59883-07-7.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 462.4 °C at 760 mmHg
• Flash Point: 169.3 °C
• Appearance: /
• Density: 1.327 g/cm³
• Vapor Pressure: 3.6E-09mmHg at 25°C
• Refractive Index: 1.621
• Storage Temp.: 2-8°C
• CAS DataBase Reference: RUBIDATE UV(CAS DataBase Reference)
• NIST Chemistry Reference: RUBIDATE UV(59883-07-7)
• EPA Substance Registry System: RUBIDATE UV(59883-07-7)

Safety Data

• Hazardous Substances Data: 59883-07-7(Hazardous Substances Data)

Usage

General Description

"Rubidate UV" is not a recognized scientific term or a known chemical compound. It could potentially be a misspelling or a brand name for a specific product. However, without additional context or accurate information, a valid summary cannot be provided. In chemistry, "Rubidium" is a chemical element on the Periodic Table with the symbol "Rb." "UV" commonly refers to ultraviolet light or radiation. Rubidium may exhibit particular properties when exposed to UV light, but "Rubidate UV" does not correspond to a specific known compound or chemical reaction. Please provide more detailed or correct information.

InChI:InChI=1/C16H16O6/c1-3-21-15(19)11-12(16(20)22-4-2)14(18)10-8-6-5-7-9(10)13(11)17/h5-8,17-18H,3-4H2,1-2H3

Upstream product

• 84-66-2 Diethyl phthalate 
• 141-52-6 sodium ethanolate 
• 123-25-1 succinic acid diethyl ester 
• 113674-51-4 2-Carbobenzoxybenzaldehyde 
• 1520-50-9 but-2-enedioic acid diethyl ester 
• 169216-80-2 1-Benzenesulfinyl-4-hydroxy-naphthalene-2,3-dicarboxylic acid diethyl ester 

Downstream Products

• 80594-13-4 Phenyl-acetic acid 3-phenylacetoxymethyl-1,4-dipropoxy-naphthalen-2-ylmethyl ester 
• 80593-95-9 1,4-bis(propynyloxy)-2,3-bis(phenylacetyloxymethyl)naphthalene 
• 80594-14-5 (4-Bromo-phenyl)-acetic acid 3-[2-(4-bromo-phenyl)-acetoxymethyl]-1,4-dipropoxy-naphthalen-2-ylmethyl ester 
• 80612-09-5 1,4-bis(propynyloxy)-2,3-bis(4-bromophenylacetyloxymethyl)naphthalene 
• 80594-06-5 C₆₈H₆₈O₁₂ 
• 80594-00-9 C₆₈H₅₂O₁₂ 
• 80594-07-6 C₆₈H₆₄Br₄O₁₂ 
• 80594-01-0 C₆₈H₄₈Br₄O₁₂ 
• 325780-78-7 ethyl [4-(4,9-diethoxy-1,3-dioxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetate 
• 945721-95-9 ethyl {4-[4,9-bis(ethyloxy)-1,3-dioxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl]-3-fluorophenyl}acetate 
• 1021167-92-9 ethyl {4-[4,9-bis(ethyloxy)-1,3-dioxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl]-3-chlorophenyl}acetate 
• 1021167-95-2 ethyl {4-[4,9-bis(ethyloxy)-1,3-dioxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl]-3-bromophenyl}acetate 
• 1028543-15-8 ethyl {4-[4,9-bis(ethyloxy)-1,3-dioxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl]-3-methylphenyl}acetate 
• 1028543-13-6 ethyl [4-[4,9-bis(ethyloxy)-1,3-dioxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl]-3-(trifluoromethyl)phenyl]acetate 

Relevant articles and documents

N-Heterocyclic carbene based catalytic platform for Hauser-Kraus annulations

The venerable Hauser-Kraus annulation is an effective and convergent method for generating oxygenated polycyclic aromatic compounds. Despite its application in complex molecule synthesis, the harsh and strongly basic conditions can limit its utility in more functionalized molecular settings. We have developed the first catalytic Hauser-Kraus annulation based on N-heterocyclic carbene catalysis that proceeds under milder conditions. We demonstrate the scope of the transformation in the presence of several functional groups. We also propose a concerted mechanism for the annulation that proceeds through a non-canonical Breslow intermediate. This journal is

NAPHTHALENE AND QUINOLINE SULFONYLUREA DERIVATIVES AS EP4 RECEPTOR ANTAGONISTS

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An Efficient Synthesis of p-Quinones utilizing a Novel Pummerer-type Rearrangement of p-Sulfinylphenols

Treatment of the p-sulfinylphenol derivatives 1 and 5 with trifluoroacetic anhydride causes a Pummerer-type rearrangement on aromatic rings and concomitant desulfurization to give 1:1 mixtures of the corresponding p-quinones and p-dihydroquinones, which are subjected to mild oxidation to provide high yields of p-quinones 3 and 7.