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4-(Phenyl-thiophen-2-yl-methyl)-phenol is an organic compound characterized by its unique molecular structure, which consists of a phenol group (a hydroxyl group attached to a benzene ring) connected to a thiophen-2-ylmethyl group (a methyl group attached to a thiophene ring, which is a benzene ring with one oxygen atom replaced by a sulfur atom). 4-(PHENYL-THIOPHEN-2-YL-METHYL)-PHENOL is also phenyl-substituted, meaning it has a benzene ring attached to the thiophen-2-ylmethyl group. The combination of these functional groups gives the compound specific chemical properties, such as potential reactivity with electrophiles due to the presence of the phenol hydroxyl group and the possibility of forming charge-transfer complexes due to the electron-rich thiophene ring. It may have applications in the synthesis of pharmaceuticals, materials science, or as a chemical intermediate in various organic reactions.

731-50-0

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731-50-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 731-50-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 731-50:
(5*7)+(4*3)+(3*1)+(2*5)+(1*0)=60
60 % 10 = 0
So 731-50-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H14OS/c18-15-10-8-14(9-11-15)17(16-7-4-12-19-16)13-5-2-1-3-6-13/h1-12,17-18H

731-50-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[phenyl(thiophen-2-yl)methyl]phenol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:731-50-0 SDS

731-50-0Downstream Products

731-50-0Relevant academic research and scientific papers

Thiophene containing trisubstituted methanes [TRSMs] as identified lead against Mycobacterium tuberculosis

Singh, Priyanka,Manna, Sudipta Kumar,Jana, Amit Kumar,Saha, Tiash,Mishra, Pankaj,Bera, Saurav,Parai, Maloy Kumar,Srinivas Lavanya Kumar,Mondal, Sankalan,Trivedi, Priyanka,Chaturvedi, Vinita,Singh, Shyam,Sinha, Sudhir,Panda, Gautam

, p. 357 - 368 (2015/04/14)

Triarylmethanes (TRAMs) and thiophene containing trisubstituted methanes (TRSMs) have been reported by us, having potential against Mycobacterium tuberculosis and Mycobacterium fortuitum strains, respectively. Further, extension through synthesis and biol

Photoreaction between 2-benzoylthiophene and phenol or indole

Perez-Prieto, Julia,Bosca, Francisco,Galian, Raquel E.,Lahoz, Agustin,Domingo, Luis R.,Miranda, Miguel A.

, p. 5104 - 5113 (2007/10/03)

Laser flash photolysis, density functional theory (DFT) calculations, and product studies have been performed to understand the mechanism of photoreduction of 2-benzoylthiophene (BT) in the presence of phenol or indole. Time-resolved experiments showed th

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