79135-62-9

Basic information

• Product Name: 1,2-bis(4-(tert-butyl)phenyl)ethan-1-one
• Synonyms: 1,2-bis(4-(tert-butyl)phenyl)ethan-1-one
• CAS NO: 79135-62-9
• Molecular Weight: 308.464
• Mol File: 79135-62-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,2-bis(4-(tert-butyl)phenyl)ethan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-bis(4-(tert-butyl)phenyl)ethan-1-one(79135-62-9)
• EPA Substance Registry System: 1,2-bis(4-(tert-butyl)phenyl)ethan-1-one(79135-62-9)

Safety Data

• Hazardous Substances Data: 79135-62-9(Hazardous Substances Data)

Upstream product

• 77387-64-5 1,2-bis((4-tert-butyl)phenyl)-2-hydroxyethanone 
• 61440-86-6 bis(4-tert-butylphenyl)acetylene 
• 1710-98-1 p-tert-butyl benzoyl chloride 
• 939-97-9 4-tert-Butylbenzaldehyde 
• 22927-07-7 1,2-bis(4-tert-butylphenyl)ethane 
• 98-51-1 4-tert-butyltoluene 
• 75966-32-4 p-tert-butyl-α,α-dibromotoluene 
• 79135-54-9 p,p'-Di-tert-butylstilbene 
• 79135-60-7 1-tert-butyl-(4-dichloromethyl)benzene 
• 79135-53-8 1-Bromo-1,2-bis(p-tert-butylphenyl)ethane 
• 79135-56-1 1,2-Dichloro-1,2-bis(p-tert-butylphenyl)ethane 
• 79135-59-4 C₂₂H₃₀N₄ 
• 79135-57-2 1,2-Dibromo-1,2-bis(p-tert-butylphenyl)ethane 
• 3972-65-4 1-bromo-4-tert-butylbenzene 

Downstream Products

• 76471-78-8 4,4'-di-tert-butylbenzil 

Relevant articles and documents

POLYCYCLIC COMPOUND AND AN ORGANIC ELECTROLUMINESCENCE DEVICE COMPRISING THE POLYCYCLIC COMPOUND OR THE COMPOSITION

Specific polycyclic compounds, a material for an organic electroluminescence device comprising said specific polycyclic compound, an organic electroluminescence device comprising said specific polycyclic compound, an electronic equipment comprising said organic electroluminescence device, a process for preparing said polycyclic compounds, and the use of said polycyclic compounds in an organic electroluminescence. (Formula I) (I)

REDUCTIVE COUPLING OF BENZOIC ACID HALIDES AND ESTERS USING LOW-VALENT TITANIUM

The reductive coupling of (substituted) benzoic acid chlorides and esters is achieved using low-valent titanium, generated from TiCl3 and LiAlH4.Both acid chlorides and esters seem to follow the same two reaction pathways: one path via tolanes to stilbenes, the other via benzils to complex mixtures of products arising from reduction and further coupling reactions.Although the exact product balance depends upon the reaction conditions the major product is (substituted) cis-stilbene.