849907-82-0

Basic information

• Product Name: Benzene, 1-ethynyl-4-(1,1,3,3-tetramethylbutyl)-
• CAS NO: 849907-82-0
• Molecular Formula: C16H22
• Molecular Weight: 214.351
• Mol File: 849907-82-0.mol

Chemical Properties

• CAS DataBase Reference: Benzene, 1-ethynyl-4-(1,1,3,3-tetramethylbutyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-ethynyl-4-(1,1,3,3-tetramethylbutyl)-(849907-82-0)
• EPA Substance Registry System: Benzene, 1-ethynyl-4-(1,1,3,3-tetramethylbutyl)-(849907-82-0)

Safety Data

• Hazardous Substances Data: 849907-82-0(Hazardous Substances Data)

Upstream product

• 140-66-9 tert-octylphenol 
• 1334015-13-2 2-methyl-4-(4-tert-octylphenyl)-but-3-yn-2-ol 
• 849907-81-9 4-tert-octyl-1-trifluoromethanesulfonyloxybenzene 

Downstream Products

• 1008747-62-3 1,5-dibromo-2,4-bis[2-[4-(1,1,3,3-tetramethylbutyl)phenyl]ethynyl]benzene 
• 1310727-09-3 2,7-bis(4-tert-octylphenylethynyl)-9,10-dimethoxyphenanthrene 
• 1310727-17-3 2,7-bis(4-tert-octylphenylethynyl)-phenanthrene-9,10-dione 
• 1310727-30-0 3,6-bis(4-tert-octylphenylethynyl)-dibenzo[a,c]phenazine 
• 1310727-36-6 2,7-bis(4-tert-octylphenylethynyl)-dibenzo[a,c]phenazine 
• 1310727-05-9 3,6-bis(4-tert-octylphenylethynyl)-9,10-dimethoxyphenanthrene 
• 1310727-13-9 3,6-bis(4-tert-octylphenylethynyl)-phenanthrene-9,10-dione 
• 849907-84-2 1-[(trimethylsilyl)ethynyl]-2-[[4-(1,1,3,3-tetramethylbutyl)phenyl]ethynyl]benzene 
• 849907-68-2 1-ethynyl-2-[[4-(1,1,3,3-tetramethylbutyl)phenyl]ethynyl]benzene 
• 1026278-10-3 1-iodo-2-[[4-(1,1,3,3-tetramethylbutyl)phenyl]ethynyl]benzene 
• 849907-83-1 1-bromo-2-[[4-(1,1,3,3-tetramethylbutyl)phenyl]ethynyl]benzene 

Relevant articles and documents

Synthesis and photophysics of dibenz[a,c]phenazine derivatives

The synthesis of dipolar dibenz[a,c]phenazine (DBP) derivatives is described. The compounds possess little electronic communication between donor and acceptor units in the ground state regardless of the pattern of substitution. The dipolar derivatives deactivate mostly via electron transfer (eT) under polar conditions. Intersystem crossing is likely to compete for S1 relaxation.

Synthesis of diindeno-fused 4H-cyclopenta[def]phenanthren-4-ones and related compounds via benzannulated enediynyl propargylic alcohols

(Chemical Equation Presented) Treatment of propargylic diols 5-7 with thionyl chloride promoted a cascade sequence of reactions leading to dichlorides 10-12 and, after reduction with tributyltin hydride, the diindeno-fused 4H-cyclopenta[def]phenanthrenes