68151-04-2

Basic information

• Product Name: (1R,2R)-1,2-dihydrotriphenylene-1,2-diol
• Synonyms: 1,2-Triphenylenediol, 1,2-dihydro-, trans-
• CAS NO: 68151-04-2
• Molecular Formula: C₁₈H₁₄O₂
• Molecular Weight: 262.3026
• Mol File: 68151-04-2.mol

Chemical Properties

• Boiling Point: 525.2°C at 760 mmHg
• Flash Point: 257.2°C
• Density: 1.367g/cm³
• Vapor Pressure: 7.35E-12mmHg at 25°C
• Refractive Index: 1.793
• CAS DataBase Reference: (1R,2R)-1,2-dihydrotriphenylene-1,2-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R)-1,2-dihydrotriphenylene-1,2-diol(68151-04-2)
• EPA Substance Registry System: (1R,2R)-1,2-dihydrotriphenylene-1,2-diol(68151-04-2)

Safety Data

• Hazardous Substances Data: 68151-04-2(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
(1R,2R)-1,2-dihydrotriphenylene-1,2-diol is used as a building block in organic synthesis for the creation of new organic compounds. Its unique chemical structure and reactivity allow for the formation of various organic compounds, making it a valuable compound in this field.
Used in Materials Science:
(1R,2R)-1,2-dihydrotriphenylene-1,2-diol is used as a precursor in the formation of new materials. Its unique chemical structure and reactivity make it a promising candidate for the development of new materials with potential applications in various industries.
Used in Polymer Formation:
As a diol, (1R,2R)-1,2-dihydrotriphenylene-1,2-diol contains two hydroxyl groups, making it potentially useful for the formation of polymers. It can be used as a monomer or a building block in the synthesis of polymers with specific properties and applications.
Overall, (1R,2R)-1,2-dihydrotriphenylene-1,2-diol is a versatile compound with potential applications in various fields, including organic synthesis, materials science, and polymer formation. Its unique chemical structure and reactivity make it a compound of interest for further research and development.

Upstream product

• 82120-28-3 triphenylene-1,2-dione 
• 108-24-7 acetic anhydride 
• 4120-76-7 9-bromo-10-hydroxyphenanthrene 
• 68151-18-8 3,4-dihydrotriphenylene 
• 68151-16-6 4-[9]phenanthryl-butyric acid 
• 68151-15-5 4-oxo-4-[9]phenanthryl-butyric acid 
• 68151-17-7 3,4-dihydrotriphenylen-1(2H)-one 
• 68151-22-4 1-Hydroxy-1,2,3,4-tetrahydrotriphenylen 
• 183968-59-4 C₃₂H₂₆O₃ 
• 183968-60-7 C₁₉H₁₂O₄ 
• 183968-58-3 10-bromo-9-phenathryl tosylate 
• 484-17-3 9-Phenanthrol 

Downstream Products

• 110902-33-5 (+)-(1S,2S)-trans-1,2-dihydroxy-1,2-dihydrotriphenylene 
• 110902-32-4 (-)-(1R,2R)-trans-1,2-dihydroxy-1,2-dihydrotriphenylene 

Relevant articles and documents

Stereocontrolled synthesis of syn- and anti-diol epoxide metabolites of triphenylene

The synthesis of both syn- and anti-diol epoxide metabolites of triphenylene has been achieved under complete stereochemical control commencing with commercially available 9-phenanthrol in 18% (9 steps) and 37% (8 steps) overall yields, respectively. The exceptionally high stereoselectivity of the dimethyldioxirane oxidation of trans-dihydrodiol having the quasi-diaxially disposed hydroxyl groups is particularly noteworthy.