77144-21-9

Basic information

• Product Name: 4-(p-Chlorophenyl)-2-hydroxy-2-methyl-3-butene
• Synonyms: 4-(p-Chlorophenyl)-2-hydroxy-2-methyl-3-butene
• CAS NO: 77144-21-9
• Molecular Weight: 196.677
• Mol File: 77144-21-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-(p-Chlorophenyl)-2-hydroxy-2-methyl-3-butene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(p-Chlorophenyl)-2-hydroxy-2-methyl-3-butene(77144-21-9)
• EPA Substance Registry System: 4-(p-Chlorophenyl)-2-hydroxy-2-methyl-3-butene(77144-21-9)

Safety Data

• Hazardous Substances Data: 77144-21-9(Hazardous Substances Data)

Upstream product

• 101671-01-6 1-nitro-2-(4-chlorophenyl)ethylene 
• 67-63-0 isopropyl alcohol 
• 917-64-6 methyl magnesium iodide 
• 24393-52-0 ethyl (E)-3-(4-chlorophenyl)prop-2-enoate 
• 30626-03-0 (3E)-4-(4-chlorophenyl)-3-buten-2-one 
• 74-88-4 methyl iodide 

Downstream Products

• 64003-74-3 2(E),4(E)-5-(p-Chlorophenyl)-3-methyl-2,4-pentadienoic acid 
• 77144-24-2 2(E),4(E)-5-(p-Chlorophenyl)-3-methyl-2,4-pentadienal 

Relevant articles and documents

Copper-Catalyzed Alkenylation of Alcohols with β-Nitrostyrenes via a Radical Addition-Elimination Process

A new method for the preparation of allylic alcohol derivatives has been developed via a radical mechanism using DTBP as the radical initiator promoted by copper salt. The C(sp3)-H bond in various alcohols, toluene derivatives, and alkanes were successfully converted into C-C bonds to yield the desired products in moderate to good yields.

A stereoselective synthesis of unsaturated phosphonates by Wittig-Horner reactions of bisphosphonylmethane with 5-aryl-(3-methyl)-2E,4E-pentadienals

A new type of unsaturaled phosphonates 5 were synthesized by the Wittig-Horner reactions of bisphosphonylmethane 4 with 5-aryl-2(E),4(E)-pentadienal and 5-aryl-3-methyl-2(E), 4(E)-pentadienal. The structures of all new compounds prepared were characterize