156023-27-7

Basic information

• Product Name: (2,6-diisopropylphenyl)acetylene
• Synonyms: (2,6-diisopropylphenyl)acetylene
• CAS NO: 156023-27-7
• Molecular Weight: 186.297
• Mol File: 156023-27-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (2,6-diisopropylphenyl)acetylene(CAS DataBase Reference)
• NIST Chemistry Reference: (2,6-diisopropylphenyl)acetylene(156023-27-7)
• EPA Substance Registry System: (2,6-diisopropylphenyl)acetylene(156023-27-7)

Safety Data

• Hazardous Substances Data: 156023-27-7(Hazardous Substances Data)

Upstream product

• 1066-54-2 trimethylsilylacetylene 
• 163704-47-0 2-iodo-1,3-diisopropylbenzene 
• 156023-25-5 1,2-dibromo-1-(2,6-diisopropylphenyl)ethane 
• 156023-23-3 1-(2,6-diisopropylphenyl)ethanol 
• 156023-24-4 2-ethenyl-1,3-bis(propan-2-yl)benzene 
• 57190-17-7 2-bromo-1,3-diisopropylbenzene 
• 24544-04-5 2,6-diisopropylbenzenamine 
• 156023-26-6 (E)-β-bromo-2,6-diisopropylstyrene 
• 917-54-4 methyllithium 
• 156023-28-8 α-bromo-2,6-diisopropylstyrene 

Downstream Products

• 1370328-75-8 3-methyl-1,4-bis(2,6-diisopropylphenyl)-1,2,3-triazolium tetrafluoroborate 
• 1263862-50-5 1,4-bis(2,6-diisopropylphenyl)-1H-[1,2,3]-triazole 
• 1443747-04-3 1,4-di(2,6-diisopropylphenyl)-3-methyl-H-1,2,3-triazolium iodide 

Relevant articles and documents

Suzuki-Miyaura cross-coupling reaction catalyzed by PEPPSI-type 1,4-di(2,6-diisopropylphenyl)-1,2,3-triazol-5-ylidene (tzIPr) palladium complex

A 1,4-di(2,6-diisopropylphenyl)-1,2,3-triazol-5-ylidene (tzIPr)-based PEPPSI-type palladium complex was developed as an excellent precatalyst for the Suzuki-Miyaura cross-coupling reaction. The complex showed high activity under mild conditions for the cross-coupling reactions between various types of aryl chlorides and aryl boronic acids regardless of the steric and electronic nature of the substrates.

CRYSTALLINE 1H-1,2,3-TRIAZOL-5-YLIDENES

The present invention provides novel and stable crystalline 1H-1,2,3 triazolium carbenes and metal complexes of 1H-1,2,3 triazolium carbenes. The present invention also provides methods of making 1H-1,2,3 triazolium carbenes and metal complexes of 1H-1,2,