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Diphenyl(thiophen-3-yl)methanol is an organic compound with the chemical formula C17H14OS. It is a derivative of benzyl alcohol, featuring two phenyl rings and a thiophene ring attached to a central carbon atom. This molecule is characterized by its unique structure, which combines the aromatic properties of phenyl groups with the heterocyclic nature of the thiophene ring. Diphenyl(thiophen-3-yl)methanol is of interest in organic chemistry and materials science due to its potential applications in the synthesis of various compounds, such as pharmaceuticals and organic semiconductors. Its chemical properties, including reactivity and stability, are influenced by the presence of the sulfur atom in the thiophene ring, which can participate in various chemical reactions, making it a versatile building block in the development of new materials and compounds.

2226-49-5

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2226-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2226-49-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,2 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2226-49:
(6*2)+(5*2)+(4*2)+(3*6)+(2*4)+(1*9)=65
65 % 10 = 5
So 2226-49-5 is a valid CAS Registry Number.

2226-49-5SDS

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 diphenyl(thiophen-3-yl)methanol

1.2 Other means of identification

Product number -
Other names 3-Thiophenemethanol,a,a-diphenyl

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:2226-49-5 SDS

2226-49-5Relevant academic research and scientific papers

Generation and reactions of heteroaromatic lithium compounds by using in-line mixer in a continuous flow microreactor system at mild conditions

Liu, Binjie,Fan, Yong,Lv, Xiaoming,Liu, Xiaofeng,Yang, Yongtai,Jia, Yu

, p. 133 - 137 (2013/03/13)

A lithium-halogen exchange reaction procedure was applied to introduce electrophilic substituents to the heteroaromatics, which exhibited potential in the syntheses of pharmaceutical intermediates. In this contribution, generation and reactions of heteroa

Selective palladium-catalysed ipso arylation of α,α- disubstituted benzo[b]thien-2-ylmethanols with aryl bromides using PCy 3 as ligand

Biro, A. Beatrix,Kotschy, Andras

, p. 1364 - 1368 (2008/09/18)

α,α-Diphenylbenzo[b]thien-2-ylmethanol was treated with a series of aryl bromides in the presence of palladium(II) acetate and tricyclohexylphosphane to give the appropriate 2-aryl-benzo[b]thiophenes in good to excellent yield with concomitant formation o

The Tris(2-thienyl)methyl Cation Problem. A Nuclear Magnetic Resonance Spectroscopic Study

Abarca, Belen,Asensio, Gregorio,Ballesteros, Rafael,Varea, Teresa

, p. 3224 - 3229 (2007/10/02)

A series of homologues of the trityl cation obtained by total or partial substitution of the phenyl rings for 2- or 3-thienyl groups has been studied by 1H and 13C NMR.In general, the spectral parameters found follow the expected trends.However, a most unexpected effect is found in the transformation of tris(2-thienyl)carbinol (1d) into tris(2-thienyl)methyl cation (2d) , since the increase of the total chemical shift (ΔΣδ) associated with the ionization is as low as 105 ppm.To account for this observation, several hypotheses are discussed including the possibility of through-space charge delocalization by the three sulfur atoms and the interaction of the thiophene rings in an alternate conformation.

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