22543-72-2

Basic information

• Product Name: (+/-)-(4-isopropylphenyl)phenylmethanol
• Synonyms: (+/-)-(4-isopropylphenyl)phenylmethanol
• CAS NO: 22543-72-2
• Molecular Weight: 226.318
• Mol File: 22543-72-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (+/-)-(4-isopropylphenyl)phenylmethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-)-(4-isopropylphenyl)phenylmethanol(22543-72-2)
• EPA Substance Registry System: (+/-)-(4-isopropylphenyl)phenylmethanol(22543-72-2)

Safety Data

• Hazardous Substances Data: 22543-72-2(Hazardous Substances Data)

Upstream product

• 3262-89-3 triphenylboroxine 
• 122-03-2 (4-isopropylbenzaldehyde) 
• 98-80-6 phenylboronic acid 
• 16152-51-5 (4-isopropylphenyl)boronic acid 
• 100-52-7 benzaldehyde 
• 100-58-3 phenylmagnesium bromide 
• 536-60-7 cuminol 
• 98-88-4 benzoyl chloride 
• 103-73-1 Phenetole 
• 18620-03-6 4-isopropylphenylmagnesium bromide 
• 18864-76-1 4-isopropylbenzophenone 

Downstream Products

• 18864-76-1 4-isopropylbenzophenone 
• 1426146-48-6 (R)-(4-isopropylphenyl)(phenyl)methyl acetate 
• 1002104-42-8 C₁₆H₁₆O₃ 

Relevant articles and documents

Bio-inspired asymmetric aldehyde arylations catalyzed by rhodium-cyclodextrin self-inclusion complexes

Transition-metal catalysts are powerful tools for carbon-carbon bond-forming reactions that are difficult to achieve using native enzymes. Enzymes that exhibit inherent selectivities and reactivities through host-guest interactions have inspired widesprea

Solvent control of product diversity in palladium-catalyzed addition of arylboronic acid to aryl aldehydes

In Pd-catalyzed arylboronic acid addition to aryl aldehydes, the expected carbinol or asymmetrical ether can be obtained as the major product by altering aqueous solvent composition. Exploiting this methodology with 2-formylbiphenyls as reaction partner, a fluorene scaffold can be readily constructed in two steps.