40310-33-6

Basic information

• Product Name: 2-Thiophenemethanol, a-(4-methoxyphenyl)-
• Synonyms: α-(4-methoxyphenyl)-2-thiophenemethanol;alfa-[(4'-methoxyphenyl)]-2-thienylmethanol;4-methoxyphenyl(2-thienyl)methanol;(4-Methoxy-phenyl)-[2]thienyl-methanol;(4-methoxy-phenyl)-thiophen-2-yl-methanol;α-[(4'-methoxyphenyl)]-2-thienylmethanol
• CAS NO: 40310-33-6
• Molecular Formula: C12H12O2S
• Molecular Weight: 220.292
• Mol File: 40310-33-6.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2-Thiophenemethanol, a-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Thiophenemethanol, a-(4-methoxyphenyl)-(40310-33-6)
• EPA Substance Registry System: 2-Thiophenemethanol, a-(4-methoxyphenyl)-(40310-33-6)

Safety Data

• Hazardous Substances Data: 40310-33-6(Hazardous Substances Data)

Upstream product

• 4160-63-8 2-(4-methoxybenzoyl)thiophene 
• 3437-95-4 2-Iodothiophene 
• 123-11-5 4-methoxy-benzaldehyde 
• 98-03-3 thiophene-2-carbaldehyde 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 188290-36-0 thiophene 
• 5713-61-1 thiophen-2-yl magnesium bromide 
• 83682-19-3 [2]thienyl sodium 

Downstream Products

• 135887-31-9 C₂₄H₂₂O₃S₂ 
• 1415210-11-5 C₁₅H₁₈O₂S 
• 1415210-10-4 C₂₅H₂₅NO₄S 
• 1582256-28-7 4-((4-methoxyphenyl)(thiophen-2-yl)methyl)aniline 
• 1582256-29-8 4-chloro-2-((4-methoxyphenyl)(thiophen-2-yl)methyl)-aniline 
• 852287-08-2 4-[(4-methoxy-phenyl)-thiophen-2-yl-methyl]-phenol 
• 852287-07-1 2-[(4-methoxy-phenyl)-thiophen-2-yl-methyl]-phenol 

Relevant articles and documents

Synthesis of arylcarbinols and/or arylketones end capped thiophene and 2,2′-bithiophene

Synthesis of arylmethanol of thiophene and 2,2′-bithiophene derivatives (4, 5, 8, 9 and 13) and the corresponding ketones (6, 10, 11 and 14) which were prepared by lithiation/addition exchange sequence on the arylbromides (2, 3 and 12) followed by trappin

Synergistic stereoselective organocatalysis with indium(III) salts

The compatibility of indium(III) Lewis acids with water and amines allows their employment in synergistic and cooperative catalysis. Stereoselective organocatalytic SN1-type reactions, in which carbenium ions are generated, are promoted by the presence of indium salts. The peculiar properties of indium salts can be exploited in organocatalysis for the design of water-compatible, benign, green processes. The development of such indium(III)-promoted organocatalytic procedures is the focus of our recent research, a summary of which is presented in this article. Georg Thieme Verlag Stuttgart.New York.

Thiophene containing triarylmethanes as antitubercular agents

A new series of thiophene containing triarylmethane derivatives were synthesized from the Friedel-Crafts alkylation of diarylcarbinols followed by incorporation of amino alkyl chains. These were evaluated against Mycobacterium tuberculosis H37Rv and showed the activity in the range of 3.12-12.5 μg/mL in vitro.