65898-38-6

Basic information

• Product Name: INDAN-5-CARBOXYLIC ACID
• Synonyms: ASINEX-REAG BAS 12968513;INDAN-5-CARBOXYLIC ACID;INDANE-5-CARBOXYLIC ACID;TIMTEC-BB SBB010435;5-indanecarboxylic acid(SALTDATA: FREE);5-Indancarboxylic acid;1H-INDENE-5-CARBOXYLIC ACID, 2,3-DIHYDRO
• CAS NO: 65898-38-6
• Molecular Formula: C₁₀H₁₀O₂
• Molecular Weight: 162.19
• Product Categories: pharmacetical
• Mol File: 65898-38-6.mol
• Article Data: 10

Chemical Properties

• Melting Point: 184 °C
• Boiling Point: 313.5°Cat760mmHg
• Flash Point: 142.9°C
• Appearance: /
• Density: 1.237g/cm³
• Vapor Pressure: 0.00021mmHg at 25°C
• Refractive Index: 1.608
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 4.44±0.20(Predicted)
• CAS DataBase Reference: INDAN-5-CARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: INDAN-5-CARBOXYLIC ACID(65898-38-6)
• EPA Substance Registry System: INDAN-5-CARBOXYLIC ACID(65898-38-6)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 65898-38-6(Hazardous Substances Data)

Usage

Uses

Indane-?5-?carboxylic Acid (cas# 65898-38-6) is a compound useful in organic synthesis.

InChI:InChI=1/C10H10O2/c11-10(12)9-5-4-7-2-1-3-8(7)6-9/h4-6H,1-3H2,(H,11,12)

Upstream product

• 4228-10-8 1-indan-5-yl-ethanone 
• 6321-58-0 2-(indan-5-carbonyl)-benzoic acid 
• 75-15-0 carbon disulfide 
• 7446-70-0 aluminium trichloride 
• 79-37-8 oxalyl dichloride 
• 496-11-7 INDANE 
• 124-38-9 carbon dioxide 
• 143287-97-2 2,3-dihydro-1H-inden-5-yl trifluoromethanesulfonate 
• 86031-43-8 methyl 5-indanecarboxylate 
• 51632-06-5 (2,3-dihydro-1H-inden-5-yl)methanol 
• 7647-01-0 hydrogenchloride 
• 51932-71-9 indan-5-carbanilide 
• 15719-64-9 methylammonium carbonate 
• 60-29-7 diethyl ether 

Downstream Products

• 528-44-9 1,2,4-benzene tricarboxylic acid 
• 86031-43-8 methyl 5-indanecarboxylate 
• 501649-52-1 5-(bromomethyl)-2,3-dihydro-1H-indene 
• 18775-43-4 (5-indanyl)acetonitrile 
• 1415470-61-9 (2S,3R,4R,5S,6R)-2-(7-bromo-6-(4-methoxybenzyl)-2,3-dihydro-1H-inden-4-yl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol 
• 1415470-65-3 (2S,3R,4R,5S,6R)-2-(7-chloro-6-(4-methoxybenzyl)-2,3-dihydro-1H-inden-4-yl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol 
• 103204-17-7 indan-5-carboxamide 
• 75412-82-7 2,3,4,5,6,7-Hexahydro-1H-indene-5-carbonyl chloride 
• 30084-91-4 indan-5-carbaldehyde 
• 23291-98-7 3-(2.3-Dihydro-1H-inden-5-yl)-propanoic acid 

Relevant articles and documents

Asymmetric Syntheses of Medicinally Important Isoindolinones (S)-PD 172938, (R)-JM 1232, and Related Structures

A unified approach for the asymmetric syntheses of medicinally important isoindolinones (S)-PD 172938 and (R)-JM 1232 has been accomplished via a Cu(I)-PYBOX-diPh catalyzed highly enantioselective (up to 99% ee) alkynylation/lactamization sequence in a one-pot fashion. The overall sequence involves one C-C and two C-N bond forming events in one pot starting from inexpensive starting material in ambient reaction conditions.

Catalytic Fehling's Reaction: An Efficient Aerobic Oxidation of Aldehyde Catalyzed by Copper in Water

The first example of homogeneous copper-catalyzed aerobic oxidation of aldehydes is reported. This method utilizes atmospheric oxygen as the sole oxidant, proceeds under extremely mild aqueous conditions, and covers a wide range of various functionalized aldehydes. Chromatography is generally not necessary for product purification.

HCV PROTEASE INHIBITORS

This invention relates to the compounds of formula (I) shown below. Each variable in formula (I) is defined in the specification. These compounds can be used to treat hepatitis C virus infection.