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5-iodo-7-methyl-6-phenyl-4-(2-tolyl)-7H-pyrrolo[2,3-d]pyrimidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1590459-95-2

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1590459-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1590459-95-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,9,0,4,5 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1590459-95:
(9*1)+(8*5)+(7*9)+(6*0)+(5*4)+(4*5)+(3*9)+(2*9)+(1*5)=202
202 % 10 = 2
So 1590459-95-2 is a valid CAS Registry Number.

1590459-95-2Relevant academic research and scientific papers

Microwave-assisted synthesis of substituted pyrrolo[2,3-d]pyrimidines

Prieur, Vanessa,Rubio-Martinez, Jaime,Font-Bardia, Merce,Guillaumet, Gerald,Pujol, M. Dolors

, p. 1514 - 1524 (2014/03/21)

A new synthetic route to triaryl pyrrolo[2,3-d]pyrimidines from common 4,6-dichloropyrimidine has been developed. The triarylated compounds are synthesized by three cross-coupling reactions using three different catalysts. The introduction of a C-6 aryl group was achieved in a two-step process under Sonogashira conditions [Pd(dba)2/CuI] followed by intramolecular cyclization, and application of Suzuki-Miyaura conditions [Pd(PPh 3)4; PdCl2(PPh3)2] led to C-4 and C-5 diarylation. This sequence allows a flexible synthetic approach to highly arylated pyrrolopyrimidines containing different aryl groups. A new synthetic route to triaryl pyrrolo[2,3-d]pyrimidines from common 4,6-dichloropyrimidine has been developed. The triarylated compounds are synthesized by three cross-coupling reactions using three different catalysts. Copyright

Microwave-Assisted Synthesis of Substituted Pyrrolo[2,3-d]pyrimidines

Prieur, Vanessa,Rubio-Martínez, Jaime,Font-Bardia, Mercè,Guillaumet, Gérald,Pujol, M. Dolors

, p. 1514 - 1524 (2015/10/05)

A new synthetic route to triaryl pyrrolo[2,3-d]pyrimidines from common 4,6-dichloropyrimidine has been developed. The triarylated compounds are synthesized by three cross-coupling reactions using three different catalysts. The introduction of a C-6 aryl group was achieved in a two-step process under Sonogashira conditions [Pd(dba)2/CuI] followed by intramolecular cyclization, and application of Suzuki-Miyaura conditions [Pd(PPh3)4; PdCl2(PPh3)2] led to C-4 and C-5 diarylation. This sequence allows a flexible synthetic approach to highly arylated pyrrolopyrimidines containing different aryl groups.

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