Cas 198554-06-2,4-[1-(1H-indol-5-ylcarbonyl)piperidin-4-yl]-6-(4-methoxybenzyl)pyrimidin-2-amine

198554-06-2

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Basic information

Product Name: 4-[1-(1H-indol-5-ylcarbonyl)piperidin-4-yl]-6-(4-methoxybenzyl)pyrimidin-2-amine
Synonyms: 4-[1-(1H-indol-5-ylcarbonyl)piperidin-4-yl]-6-(4-methoxybenzyl)pyrimidin-2-amine
CAS NO:198554-06-2
Molecular Formula:
Molecular Weight: 441.533
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-[1-(1H-indol-5-ylcarbonyl)piperidin-4-yl]-6-(4-methoxybenzyl)pyrimidin-2-amine(CAS DataBase Reference)
NIST Chemistry Reference: 4-[1-(1H-indol-5-ylcarbonyl)piperidin-4-yl]-6-(4-methoxybenzyl)pyrimidin-2-amine(198554-06-2)
EPA Substance Registry System: 4-[1-(1H-indol-5-ylcarbonyl)piperidin-4-yl]-6-(4-methoxybenzyl)pyrimidin-2-amine(198554-06-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 198554-06-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 198554-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,5,5 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 198554-06:
(8*1)+(7*9)+(6*8)+(5*5)+(4*5)+(3*4)+(2*0)+(1*6)=182
182 % 10 = 2
So 198554-06-2 is a valid CAS Registry Number.

198554-06-2Upstream product

198554-06-2Downstream Products

198554-06-2Relevant academic research and scientific papers

Novel piperidinylpyrimidine derivatives as inhibitors of HIV-1 LTR activation

Fujiwara, Norio,Nakajima, Takashi,Ueda, Yutaka,Fujita, Hitoshi,Kawakami, Hajime

experimental part, p. 9804 - 9816 (2009/04/06)

Piperidinylpyrimidine derivatives, previously prepared as inhibitors of TNF-α production, were evaluated for their inhibitory activity against HIV-1 LTR activation. Some of these derivatives inhibited activation of HIV-1 LTR-directed CAT gene expression i

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