408526-05-6

Basic information

• Product Name: 1,1-bis(p-chlorophenyl)-3-phenylpropargyl alcohol
• Synonyms: 1,1-bis(p-chlorophenyl)-3-phenylpropargyl alcohol
• CAS NO: 408526-05-6
• Molecular Weight: 353.248
• Mol File: 408526-05-6.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 1,1-bis(p-chlorophenyl)-3-phenylpropargyl alcohol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-bis(p-chlorophenyl)-3-phenylpropargyl alcohol(408526-05-6)
• EPA Substance Registry System: 1,1-bis(p-chlorophenyl)-3-phenylpropargyl alcohol(408526-05-6)

Safety Data

• Hazardous Substances Data: 408526-05-6(Hazardous Substances Data)

Upstream product

• 1004-22-4 (phenylethynyl)sodium 
• 90-98-2 4,4'-Dichlorobenzophenone 
• 536-74-3 phenylacetylene 

Downstream Products

• 57077-15-3 3,3-bis(4-chlorophenyl)-1-phenylprop-2-en-1-one 
• 1092071-66-3 C₅₀H₃₄Cl₂ 
• 1192167-51-3 1,1-bis(4-chlorophenyl)-5,7-dimethyl-3-phenyl-1H-inden-6-ol 
• 1266570-29-9 diethyl 3,3-bis(4-chlorophenyl)-1-phenylpropa-1,2-dienyl(4-methoxyphenyl)phosphoramidate 
• 1434146-85-6 6,6-bis(4-chlorophenyl)-3-(1,3-dithiolan-2-ylidene)-4-phenyl-1,6-dihydropyridin-2(3H)-one 
• 1434146-95-8 6,6-bis(4-chlorophenyl)-3-(1,3-dithiolan-2-ylidene)-4-phenyl-3,6-dihydro-2H-pyran-2-one 
• 1434147-08-6 1-(1,1-bis(4-chlorophenyl)-1H-inden-3-yl)-1-(1,3-dithiolan-2-ylidene)propan-2-one 
• 1434147-01-9 6,6-bis(4-chlorophenyl)-3-(1,3-dithian-2-ylidene)-4-phenyl-1,6-dihydropyridin-2(3H)-one 
• 1418213-85-0 C₃₈H₂₅Cl₂NO₃ 
• 1415035-17-4 5,5-bis(4-chlorophenyl)-4-iodo-3-phenyl-2-tosyl-2,5-dihydroisoxazole 
• 1415035-03-8 5,5-Bis(4-chlorophenyl)-3-phenyl-2-tosyl-2,5-dihydroisoxazole 
• 1242072-89-4 4-(bis(4-chlorophenyl)methyl)-2-methyl-5-phenylthiazole 

Relevant articles and documents

A metal-free tandem dehydrogenative α-arylation reaction of propargylic alcohols with 2-alkynylbenzaldoximes toward the synthesis of α-(4-bromo-isoquinolin-1-yl)-propenone skeletons

A tandem reaction of 2-alkynylbenzaldoximes with propargylic alcohols has been developed for the synthesis of α-(4-bromo-isoquinolin-1-yl)-propenones. Employing 2-alkynylbenzaldoximes as a precursor in the presence of Br2 generates 4-bromo-isoquinoline-N-

Lewis Acid-Catalyzed Formal [3+3] Annulation of Propargylic Alcohols with 4-Hydroxy-2H-chromen-2-ones

A Lewis acid-catalyzed formal [3+3] cascade annulation strategy for the formation of diverse tricyclic compounds possessing functionalized pyrano[3,2-c]chromen-5(2H)-one fragments has been developed using propargylic alcohols and 4-hydroxy-2H-chromen-2-on

Transition-Metal-Free, Br?nsted Acid-Mediated Cascade Sequence in the Reaction of Propargyl Alcohols with Sulfonamido-indoles/-indolines: Highly Substituted δ- And α-Carbolines

Br?nsted acid-mediated, transition-metal-free reaction of propargyl alcohols with sulfonamido-indoles/-indolines under mild conditions affords highly substituted δ- or α-carbolines in good to excellent yields. This protocol involves cascade reaction seque