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2-Pyrimidinamine, 4-(4-methoxyphenyl)-6-(3,4,5-trimethoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

182363-41-3

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182363-41-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 182363-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,3,6 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 182363-41:
(8*1)+(7*8)+(6*2)+(5*3)+(4*6)+(3*3)+(2*4)+(1*1)=133
133 % 10 = 3
So 182363-41-3 is a valid CAS Registry Number.

182363-41-3Downstream Products

182363-41-3Relevant academic research and scientific papers

Synthesis and biological evaluation of pyrimidine bridged combretastatin derivatives as potential anticancer agents and mechanistic studies

Kumar, Bhupinder,Sharma, Praveen,Gupta, Vivek Prakash,Khullar, Madhu,Singh, Sandeep,Dogra, Nilambra,Kumar, Vinod

, p. 130 - 140 (2018/03/23)

A number of pyrimidine bridged combretastatin derivatives were designed, synthesized and evaluated for anticancer activities against breast cancer (MCF-7) and lung cancer (A549) cell lines using MTT assays. Most of the synthesized compounds displayed good

Synthesis and biological evaluation of substituted 4,6-diarylpyrimidines and 3,5-diphenyl-4,5-dihydro-1H-pyrazoles as anti-tubercular agents

Pathak, Vinay,Maurya, Hardesh K.,Sharma, Sandeep,Srivastava, Kishore K.,Gupta, Atul

, p. 2892 - 2896 (2014/06/10)

Various substituted 4,6-diarylpyrimidin-2-amine (4), 4,6-diaryl-2- (heteroaryl)pyrimidine (6) and 1-(3,5-diaryl-4,5-dihydro-1H-pyrazol-1-yl) ethanone (7) derivatives were synthesized in good yields using simple methodology. The synthesized compounds (4-7)

Fused heterocyclic ring systems from amino- and thioxo-pyrimidine derivatives

Mahmoud,Abd-El-Halim,Ebrahim, Awatef E. F.,Radwan

, p. 915 - 919 (2007/10/03)

1-(p-Anisyl)-3-(3′, 4′, 5′-trimethoxyphenyl)prop-2-en-1-one (1) when reacts with guanidine hydrochloride and thiourea yields aminopyrimidine 2 and pyrimidinethione 8, respectively. The behaviour of 2 and 8 towards some electrophiles and nitrogen nucleophiles has been investigated.

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