67528-23-8

Basic information

• Product Name: (1R,2R)-Indan-1,2-diol, 97%
• Synonyms: (1R,2R)-Indan-1,2-diol, 97%
• CAS NO: 67528-23-8
• Molecular Formula: C₉H₁₀O₂
• Molecular Weight: 150.1745
• Mol File: 67528-23-8.mol
• Article Data: 66

Chemical Properties

• Melting Point: 184-186 °C
• Boiling Point: 288.5±40.0 °C(Predicted)
• Appearance: /
• Density: 1.334±0.06 g/cm3(Predicted)
• PKA: 13.70±0.40(Predicted)
• CAS DataBase Reference: (1R,2R)-Indan-1,2-diol, 97%(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R)-Indan-1,2-diol, 97%(67528-23-8)
• EPA Substance Registry System: (1R,2R)-Indan-1,2-diol, 97%(67528-23-8)

Safety Data

• Hazardous Substances Data: 67528-23-8(Hazardous Substances Data)

Usage

General Description

(1R,2R)-Indan-1,2-diol, 97% is a chemical compound with the molecular formula C9H10O2. It is a colorless, crystalline solid that is commonly used in the pharmaceutical and chemical industries as a chiral synthon in the synthesis of various chiral molecules. (1R,2R)-Indan-1,2-diol, 97% is highly pure, with a concentration of 97%, making it suitable for use in high-precision chemical reactions. Its chiral nature makes it a valuable building block for the creation of complex organic compounds with specific stereochemistry, and its high purity makes it a reliable and consistent reagent for chemical synthesis. Additionally, (1R,2R)-Indan-1,2-diol has potential applications in the development of new drugs and other advanced materials due to its unique chemical properties.

Upstream product

• 95-13-6 1-indene 
• 108-05-4 vinyl acetate 
• 4370-02-9 cis-indane-1,2-diol 
• 24329-96-2 2-iodoindane 
• 1579-15-3 2-acetoxyindan-1-one 
• 182575-38-8 (-)-(R)-2,3-dihydro-1-oxo-1H-inden-2-yl acetate 
• 206764-38-7 (2S)-1-Oxodihydroinden-2-yl acetate 
• 146235-25-8 (2R)-2-acetoxy-3-phenylpropanoic acid 
• 347850-57-1 (R)-1-chloro-1-oxo-3-phenylpropan-2-yl acetate 
• 7529-22-8 4-methylmorpholine N-oxide 
• 768-22-9 2,3-epoxyindene 
• 67-56-1 methanol 
• 19597-99-0 2-Formyl-1,2-indanadiol 
• 10368-44-2 trans-2-bromo-1-indanol 

Downstream Products

• 615-13-4 2-indanone 
• 25705-34-4 2-(2-oxoethyl)benzaldehyde 
• 4370-02-9 cis-indane-1,2-diol 
• 19597-96-7 syn-2,3-dihydro-1H-indene-1,2-diyl diacetate 
• 88270-69-3 anti-2,3-dihydro-1H-indene-1,2-diyl diacetate 
• 19458-28-7 2-butyl-(3ar,8ac)-8,8a-dihydro-3aH-indeno[1,2-d][1,3,2]dioxaborole 
• 4370-02-9 trans-indane-1,2-diol 
• 144730-60-9 3,4-dihydro-1H-2-benzopyran-1,3-diol 
• 1579-16-4 2-hydroxyindan-1-one 
• 109296-68-6 1-hydroxy-2-indanone 
• 4370-02-9 (1R,2S)-indane-1,2-diol 
• 4370-02-9 cis-1,2-indandiol 
• 19597-99-0 2-Formyl-1,2-indanadiol 
• 175166-51-5 (3aS,3a'S,8aR,8a'R)-2,2'-(propane-2,2-diyl)bis(3a,8a-dihydro-8H-indeno[1,2-d]oxazole) 

Relevant articles and documents

Regioselective biocatalytic self-sufficient Tishchenko-type reactionviaformal intramolecular hydride transfer

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Controlling Selectivity in Alkene Oxidation: Anion Driven Epoxidation or Dihydroxylation Catalysed by [Iron(III)(Pyridine-Containing Ligand)] Complexes

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A de Novo Synthetic Route to 1,2,3,4-Tetrahydroisoquinoline Derivatives

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