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2,3-dimethyl-5-phenylpyrazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1391986-79-0

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1391986-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1391986-79-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,1,9,8 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1391986-79:
(9*1)+(8*3)+(7*9)+(6*1)+(5*9)+(4*8)+(3*6)+(2*7)+(1*9)=220
220 % 10 = 0
So 1391986-79-0 is a valid CAS Registry Number.

1391986-79-0Downstream Products

1391986-79-0Relevant academic research and scientific papers

Metal free C-H functionalization of diazines and related heteroarenes with organoboron species and its application in the synthesis of a CDK inhibitor, meriolin 1

Thatikonda, Thanusha,Singh, Umed,Ambala, Srinivas,Vishwakarma, Ram A.,Singh, Parvinder Pal

, p. 4312 - 4320 (2016)

Here, we report a metal-free cross-coupling reaction of diazines and related heteroarenes with organoboron species via C-H functionalization. The optimized conditions represent a metal-free method for the activation of aryl/heteroarylboronic acids, which undergo coupling with diazines and related heteroarenes. Optimized conditions also find application in the synthesis of a pyrimidine-based potent CDK inhibitor, meriolin1.

Regioselective synthesis of trialkylpyrazines via nickel-catalyzed Negishi cross-coupling of pyrazine triflate

Pitchaiah, Arigala,Hwang, Intaek,Hwang, Jin-Soo,Kim, Hyungrok,Lee, Kee-In

, p. 1631 - 1636 (2012/06/30)

A regioselective synthesis of trialkylpyrazines via nickel-catalyzed cross-coupling reaction of pyrazine triflate is reported. The 5-substituted 2,3-dimethylpyrazine derivatives including trail pheromone components of the ant Eutetramorium mocquerysi have been successfully synthesized in good yields by nickel-catalyzed Negishi cross-coupling reactions of pyrazine triflate mediated by alkyl and arylzinc halides. Georg Thieme Verlag Stuttgart · New York.

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