64401-21-4

Basic information

• Product Name: PYRENE,1,3-DIMETHYL-
• Synonyms: PYRENE,1,3-DIMETHYL-
• CAS NO: 64401-21-4
• Molecular Formula: C₁₈H₁₄
• Molecular Weight: 230.3038
• Mol File: 64401-21-4.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 401.7 °C at 760 mmHg
• Flash Point: 188.5 °C
• Appearance: /
• Density: 1.183g/cm³
• Vapor Pressure: 2.69E-06mmHg at 25°C
• Refractive Index: 1.786
• CAS DataBase Reference: PYRENE,1,3-DIMETHYL-(CAS DataBase Reference)
• NIST Chemistry Reference: PYRENE,1,3-DIMETHYL-(64401-21-4)
• EPA Substance Registry System: PYRENE,1,3-DIMETHYL-(64401-21-4)

Safety Data

• Hazardous Substances Data: 64401-21-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C18H14/c1-11-10-12(2)16-9-7-14-5-3-4-13-6-8-15(11)18(16)17(13)14/h3-10H,1-2H3

Upstream product

• 108-88-3 toluene 
• 155386-59-7 7-(tert-butyl)-1,3-dimethylpyrene 
• 129-00-0 pyrene 
• 1005771-04-9 1,3-dibromo-7-(tert-butyl)pyrene 
• 155386-77-9 syn-6,17-di-tert-butyl-9-methoxy-2,11-dithia<3>metacyclo<3>(1,3)pyrenophane S,S,S',S'-tetraoxide 
• 155386-76-8 anti-6,17-di-tert-butyl-9-ethyl-2,11-dithia<3>metacyclo<3>(1,3)pyrenophane S,S,S',S'-tetraoxide 
• 155386-78-0 syn-6,17-di-tert-butyl-9-fluoro-2,11-dithia<3>metacyclo<3>(1,3)pyrenophane S,S,S',S'-tetraoxide 
• 155386-75-7 anti-6,17-di-tert-butyl-9-methyl-2,11-dithia<3>metacyclo<3>(1,3)pyrenophane S,S,S',S'-tetraoxide 
• 155386-64-4 anti-8-tert-butyl-2,15-dithia<3>metacyclo<3>(1,3)pyrenophane S,S,S',S'-tetraoxide 
• 155386-73-5 syn-6,17-di-tert-butyl-9-methoxy-2,11-dithia<3>metacyclo<3>(1,3)pyrenophane 
• 155386-74-6 syn-6,17-di-tert-butyl-9-fluoro-2,11-dithia<3>metacyclo<3>(1,3)pyrenophane 
• 155386-72-4 anti-6,17-di-tert-butyl-9-ethyl-2,11-dithia<3>metacyclo<3>(1,3)pyrenophane 
• 155386-66-6 anti-6,17-di-tert-butyl-9-methyl-2,11-dithia<3>metacyclo<3>(1,3)pyrenophane 
• 155386-63-3 syn-8-tert-butyl-2,15-dithia<3>metacyclo<3>(1,3)pyrenophane 

Relevant articles and documents

Extremely Active Organocatalysts Enable a Highly Enantioselective Addition of Allyltrimethylsilane to Aldehydes

The enantioselective allylation of aldehydes to form homoallylic alcohols is one of the most frequently used carbon–carbon bond-forming reaction in chemical synthesis and, for several decades, has been a testing ground for new asymmetric methodology. Howe

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Synthesis of 1,2-Dimethylpyrene, 1,3-Dimethylpyrene and 1,2,3-Trimethylpyrene

The title compounds have been prepared, starting from 1H-phenalene 1.The method described in this paper is an efficient procedure for introducing methyl groups into the A-ring of pyrene.