Cas 293292-20-3,2-{4-[2-Hydroxy-3-(N,N-dimethylamino)propoxy]anilino}-4-(indol-1-yl)-5-methylpyrimidine

293292-20-3

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Basic information

Product Name: 2-{4-[2-Hydroxy-3-(N,N-dimethylamino)propoxy]anilino}-4-(indol-1-yl)-5-methylpyrimidine
Synonyms: 2-{4-[2-Hydroxy-3-(N,N-dimethylamino)propoxy]anilino}-4-(indol-1-yl)-5-methylpyrimidine
CAS NO:293292-20-3
Molecular Formula:
Molecular Weight: 417.511
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: 2-{4-[2-Hydroxy-3-(N,N-dimethylamino)propoxy]anilino}-4-(indol-1-yl)-5-methylpyrimidine(CAS DataBase Reference)
NIST Chemistry Reference: 2-{4-[2-Hydroxy-3-(N,N-dimethylamino)propoxy]anilino}-4-(indol-1-yl)-5-methylpyrimidine(293292-20-3)
EPA Substance Registry System: 2-{4-[2-Hydroxy-3-(N,N-dimethylamino)propoxy]anilino}-4-(indol-1-yl)-5-methylpyrimidine(293292-20-3)

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: 293292-20-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 293292-20-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,3,2,9 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 293292-20:
(8*2)+(7*9)+(6*3)+(5*2)+(4*9)+(3*2)+(2*2)+(1*0)=153
153 % 10 = 3
So 293292-20-3 is a valid CAS Registry Number.

293292-20-3Upstream product

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293292-20-3Relevant academic research and scientific papers

PYRIMIDINE COMPOUNDS

-

, (2008/06/13)

A pyrimidine derivative of formula (I) or (I'): wherein: Ris a substituent as defined within; Q1 is optionally substituted phenyl, and Q1 bears a substituent of formula (Ia) wherein: X, Y, Y, Z, n, and m are as defined within; -NQ2 is an optionally substituted heterocyclic moiety containing one hydrogen heteroatom and optionally containing a further heteroatom; or a pharmaceutically acceptable salt in vivo hydrolysable ester thereof; are useful as anti-cancer agents. Processes for their manufacture and pharmaceutical compositions containing them are described.

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