Cas 240496-93-9,4-[1-(1,3-benzodioxol-5-ylcarbonyl)piperidin-4-yl]-5-(4-methoxyphenyl)-6-methylpyrimidin-2-amine

240496-93-9

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Basic information

Product Name: 4-[1-(1,3-benzodioxol-5-ylcarbonyl)piperidin-4-yl]-5-(4-methoxyphenyl)-6-methylpyrimidin-2-amine
Synonyms: 4-[1-(1,3-benzodioxol-5-ylcarbonyl)piperidin-4-yl]-5-(4-methoxyphenyl)-6-methylpyrimidin-2-amine
CAS NO:240496-93-9
Molecular Formula:
Molecular Weight: 446.506
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-(1,3-benzodioxol-5-ylcarbonyl)piperidin-4-yl]-5-(4-methoxyphenyl)-6-methylpyrimidin-2-amine(CAS DataBase Reference)
NIST Chemistry Reference: 4-[1-(1,3-benzodioxol-5-ylcarbonyl)piperidin-4-yl]-5-(4-methoxyphenyl)-6-methylpyrimidin-2-amine(240496-93-9)
EPA Substance Registry System: 4-[1-(1,3-benzodioxol-5-ylcarbonyl)piperidin-4-yl]-5-(4-methoxyphenyl)-6-methylpyrimidin-2-amine(240496-93-9)

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: 240496-93-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 240496-93-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,0,4,9 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 240496-93:
(8*2)+(7*4)+(6*0)+(5*4)+(4*9)+(3*6)+(2*9)+(1*3)=139
139 % 10 = 9
So 240496-93-9 is a valid CAS Registry Number.

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240496-93-9Relevant 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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