76376-91-5

Basic information

• Product Name: Benzene, (heptylseleno)-
• CAS NO: 76376-91-5
• Molecular Formula: C13H20Se
• Molecular Weight: 255.262
• Mol File: 76376-91-5.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzene, (heptylseleno)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, (heptylseleno)-(76376-91-5)
• EPA Substance Registry System: Benzene, (heptylseleno)-(76376-91-5)

Safety Data

• Hazardous Substances Data: 76376-91-5(Hazardous Substances Data)

Upstream product

• 71098-88-9 N-phenylselanylphthalimide 
• 111-70-6 n-heptan1ol 
• 629-06-1 1-Chloroheptane 
• 23974-72-3 sodium phenylselenide 
• 60221-21-8 1,1-bis(phenylseleno)heptane 
• 100-52-7 benzaldehyde 
• 629-04-9 1-Bromoheptane 
• 1666-13-3 diphenyl diselenide 
• 4282-40-0 1-Iodoheptane 
• 1331914-09-0 heptyldiphenylphosphinite 

Downstream Products

• 91-01-0 1,1-Diphenylmethanol 
• 19396-73-7 1-phenyloctan-1-ol 
• 52056-02-7 diheptyl selenide 
• 92368-72-4 1-heptyl-4-methoxybenzene 
• 101262-02-6 2-heptyl-1,4-dimethoxybenzene 
• 131568-28-0 4-heptyl-1,2-dimethoxybenzene 

Relevant articles and documents

Mechanistic Insight into the Oxidation of Organic Phenylselenides by H2O2

The oxidation of organic phenylselenides by H2O2is investigated in model compounds, namely, n-butyl phenyl selenide (PhSe(nBu)), bis(phenylselanyl)methane (PhSeMeSePh), diphenyl diselenide (PhSeSePh), and 1,2-bis(phenylselanyl)ethane

P -Selective (sp2)-C-H functionalization for an acylation/alkylation reaction using organic photoredox catalysis

p-Selective (sp2)-C-H functionalization of electron rich arenes has been achieved for acylation and alkylation reactions, respectively, with acyl/alkylselenides by organic photoredox catalysis involving an interesting mechanistic pathway.

A mild and efficient method for preparing alkyl phenyl selenides from alkyl diphenyl phosphinites

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