7470-14-6

Basic information

• Product Name: 3-PHENANTHRENECARBOXYLIC ACID
• Synonyms: 3-PHENANTHRENECARBOXYLIC ACID;Phenanthrene-3-carboxylic acid
• CAS NO: 7470-14-6
• Molecular Formula: C₁₅H₁₀O₂
• Molecular Weight: 222.24
• EINECS: 200-258-5
• Mol File: 7470-14-6.mol
• Article Data: 8

Chemical Properties

• Melting Point: 270 °C
• Boiling Point: 435.4 °C at 760 mmHg
• Flash Point: 194.8 °C
• Appearance: /
• Density: 1.305 g/cm³
• Vapor Pressure: 2.37E-08mmHg at 25°C
• Refractive Index: 1.743
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: DMSO (Slightly), Methanol (Very Slightly, Heated)
• PKA: 4.20±0.30(Predicted)
• CAS DataBase Reference: 3-PHENANTHRENECARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-PHENANTHRENECARBOXYLIC ACID(7470-14-6)
• EPA Substance Registry System: 3-PHENANTHRENECARBOXYLIC ACID(7470-14-6)

Safety Data

• Hazardous Substances Data: 7470-14-6(Hazardous Substances Data)

Usage

Uses

3-Phenanthrenecarboxylic Acid is a useful building block.

InChI:InChI=1/C15H10O2/c16-15(17)12-8-7-11-6-5-10-3-1-2-4-13(10)14(11)9-12/h1-9H,(H,16,17)

Upstream product

• 79-37-8 oxalyl dichloride 
• 85-01-8 phenanthrene 
• 715-50-4 3-bromophenanthrene 
• 2039-76-1 1-(phenanthren-3-yl)ethanone 
• 21661-50-7 phenanthrene-3-carbonitrile 
• 5345-98-2 methyl 3-phenanthrenecarboxylate 
• 108478-52-0 1,2,3,4-tetrahydro-phenanthrene-3-carboxylic acid 
• 128318-37-6 (RS)-(1-naphthylmethyl)succinic acid 
• 106595-32-8 1-oxo-1,2,3,4-tetrahydro-phenanthrene-3-carboxylic acid 

Downstream Products

• 124-38-9 carbon dioxide 
• 85-01-8 phenanthrene 
• 32155-34-3 phenanthrenequinone-3-carboxylic acid 
• 344768-30-5 (2RS,3SR)-1-(phenanthren-3-ylcarbonyl)piperazine-2,3-dicarboxylic acid 
• 7466-50-4 phenanthrene-3-carbaldehyde 

Relevant articles and documents

Ultrafast Photoclick Reaction for Selective18F-Positron Emission Tomography Tracer Synthesis in Flow

The development of very fast, clean, and selective methods for indirect labeling in PET tracer synthesis is an ongoing challenge. Here we present the development of an ultrafast photoclick method for the synthesis of short-lived18F-PET tracers

COMPOSITIONS AND METHODS OF MAKING EXPANDED HEMATOPOIETIC STEM CELLS USING PTEN INHIBITORS

This invention is directed to, inter alia, compounds, methods, systems, and compositions for the maintenance, enhancement, and expansion of hematopoietic stem cells derived from sources of non-mobilized peripheral blood. Also provided herein are compounds of Formula I which are useful in maintaining, enhancing, and expanding of hematopoietic stem cells.

Preparation of polycyclic azaarenes by an extended Pomeranz-Fritsch procedure

An extension of the Pomeranz-Fritsch procedure has been evaluated as a route to some polycyclic azaarenes. Aromatic aldehydes were treated with the dimethyl and diethyl acetals of 2-aminoethanal, the resulting imines reduced to amines which were tosylated and the resulting sulfonamides treated under a range of acidic conditions. The two naphthaldehydes led to benzo[f]isoquinoline and benzo[h]isoquinoline in overall yields of 13% and 36%. Phenanthrene-9- carbaldehyde and phenanthrene-3-carbaldehyde gave dibenzo[f,h]isoquinoline and naphtho[2,1-g]isoquinoline, respectively, as the major tetracyclic products. No pentacyclic product was obtained from a similar sequence starting from pyrene-1-carbaldehyde. Georg Thieme Verlag Stuttgart.