36944-99-7

Basic information

• Product Name: 5-Methyl-2-phenylindolizine
• Synonyms: 5-Methyl-2-phenylindolizine
• CAS NO: 36944-99-7
• Molecular Formula: C₁₅H₁₃N
• Molecular Weight: 207.27
• Mol File: 36944-99-7.mol
• Article Data: 4

Chemical Properties

• Melting Point: 83-83.5 °C
• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.04g/cm³
• Refractive Index: 1.599
• CAS DataBase Reference: 5-Methyl-2-phenylindolizine(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Methyl-2-phenylindolizine(36944-99-7)
• EPA Substance Registry System: 5-Methyl-2-phenylindolizine(36944-99-7)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 36944-99-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H13N/c1-12-6-5-9-15-10-14(11-16(12)15)13-7-3-2-4-8-13/h2-11H,1H3

Upstream product

• 109510-06-7 3-(6-methyl-[2]pyridyl)-2-phenyl-propan-1-ol 
• 108-48-5 2,6-dimethylpyridine 
• 621-82-9 Cinnamic acid 
• 875250-74-1 2,6-lutidyllithium 
• 96-09-3 styrene oxide 
• 81071-62-7 3-ethoxalyl-5-methyl-2-phenylindolizine 
• 25379-20-8 2-phenylindolizine 
• 74-88-4 methyl iodide 
• 70-11-1 α-bromoacetophenone 

Downstream Products

• 138611-49-1 tetramethyl 5,6,7,8,9,9a-hexahydro-9a-methyl-3-phenylazocino<2.1.8-cd>pyrrolizine-1,2,5,6-tetracarboxylate 
• 81071-68-3 (4-Methoxy-3-oxo-2-phenyl-3H-pyrrolo[2,1,5-de]quinolizin-1-yl)-oxo-acetic acid ethyl ester 
• 81071-67-2 1-ethoxalyl-4-hydroxy-2-phenyl-3H-<2.3.3>cyclazin-3-one 
• 81071-95-6 4-Oxalyl-3-phenyl-pyrrolo[2,1,5-cd]indolizine-2-carboxylic acid 
• 81071-94-5 (4-Hydroxy-3-oxo-2-phenyl-3H-pyrrolo[2,1,5-de]quinolizin-1-yl)-oxo-acetic acid 
• 81071-96-7 4-Hydroxy-3-oxo-2-phenyl-3H-pyrrolo[2,1,5-de]quinolizine-1-carboxylic acid 
• 81071-70-7 2-phenylpyrrolo<2,1,5-cd>indolizine-1,3-dicarboxylic acid 
• 81071-66-1 ethyl 3-phenyl<2.2.3>cyclazine-2-carboxylate 
• 81071-90-1 2,4-phenyl-3H-pyrrolo<2,1,5-de>quinolizine-3-one 
• 81071-91-2 4-methyl-2-phenyl-3H-pyrrolo<2,1,5-de>quinolizine-3-thione 
• 81071-75-2 4-methyl-2-phenyl-3H-<2.3.3>cyclazin-3-one 
• 81071-69-4 ethyl 4-ethoxalyl-3-phenyl<2.2.3>cyclazine-2-carboxylate 
• 49618-63-5 3-phenyl-pyrrolo[2,1,5-cd]indolizine-2-carboxylic acid 
• 14807-48-8 2-phenyl-4-hydroxy-3H-pyrrolo<2,1,5-de>quinolizin-3-one 

Relevant articles and documents

Ruthenium-NHC-Catalyzed asymmetric hydrogenation of indolizines: Access to indolizidine alkaloids

Crossing N-bridges! A ruthenium/N-heterocyclic carbene (NHC) complex serves as the catalyst for the high-yielding and completely regioselective and asymmetric hydrogenation of substituted indolizines and 1,2,3-triazolo-[1,5-a] pyridines. This method shoul

Metallation of 2-phenylindolizine

Regioselective metallation of 2-phenylindolizine at C(5) and subsequent reaction with an electrophile has afforded the corresponding C(5) functionalised indolizine in high yields.