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2,2'-Bithiophene,5-methyl-5'-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106925-68-2

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106925-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106925-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,9,2 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 106925-68:
(8*1)+(7*0)+(6*6)+(5*9)+(4*2)+(3*5)+(2*6)+(1*8)=132
132 % 10 = 2
So 106925-68-2 is a valid CAS Registry Number.

106925-68-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-5-(5-phenylthiophen-2-yl)thiophene

1.2 Other means of identification

Product number -
Other names 5-methyl-5'-phenyl-2,2'-bithiophene

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:106925-68-2 SDS

106925-68-2Downstream Products

106925-68-2Relevant academic research and scientific papers

Factors controlling the reactivity of heteroarenes in direct arylation with arylpalladium acetate complexes

Wakioka, Masayuki,Nakamura, Yuki,Hihara, Yoshihiro,Ozawa, Fumiyuki,Sakaki, Shigeyoshi

, p. 4423 - 4430 (2013/09/02)

The palladium-catalyzed direct arylation of heteroarenes with aryl halides has emerged as a viable alternative to conventional cross-coupling reactions. This paper reports a detailed mechanistic study on factors controlling the reactivity of heteroarenes in direct arylation with well-defined models of the presumed intermediate [PdAr(O2CMe-κ2O)L] (1). Although recent theoretical studies have provided a reasonable description of the mechanism of C-H bond cleavage by 1, its model compounds so far tested have been evidently less reactive than that expected. We found that [PdPh(O 2CMe-κ2O)(PPh3)] (1a) and [Pd(2,6-Me 2C6H3)(O2CMe-κ2O) (PPh3)] (1c), generated in situ from isolated [PdPh(μ-O 2CMe)(PPh3)]2 (4a) and [Pd(2,6-Me 2C6H3)(μ-O2CMe)(PPh 3)]4 (4c), respectively, react with a variety of heteroarenes in almost quantitative yields. The reactivity order of heteroarenes was evaluated by competitive reactions, showing that benzothiazole (8) is significantly less reactive than 2-methylthiophene (6), despite the acidity of 8 (pKa = 27) being much higher than that of 6 (pKa = 42). This reason was examined by kinetic experiments using 1c as well as DFT calculations using the model compound [PdPh(O2CMe- κ2O)(PH3)] (1d). Both heteroarenes reacted with 1 via a sequence of three elementary processes (i.e., substrate coordination, C-H bond cleavage, and C-C reductive elimination), but their energy profiles were significantly different from each other. The reaction of 6 obeyed simple second-order kinetics, and the deuterium-labeling experiments and DFT calculations indicated the occurrence of rate-determining reductive elimination. On the other hand, the reaction of 8 displayed saturation kinetics due to the occurrence of relatively stable coordination of 8 prior to C-H bond cleavage. This coordination stability enhances the activation barrier for C-H bond cleavage, thereby causing the modest reactivity of 8. Thus, although the previous mechanistic studies on direct arylation have been focused largely on the C-H bond cleavage process, not only the C-H bond cleavage but also the substrate coordination and C-C reductive elimination must be considered.

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