Cas 403791-08-2,2-Pyrimidinamine, N-(3-chlorophenyl)-4-[1-(2-methoxyethyl)-1H-imidazol-5-yl]-, monohydrochloride

403791-08-2

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Basic information

Product Name: 2-Pyrimidinamine, N-(3-chlorophenyl)-4-[1-(2-methoxyethyl)-1H-imidazol-5-yl]-, monohydrochloride
Synonyms:
CAS NO:403791-08-2
Molecular Formula: C16H16ClN5O.ClH
Molecular Weight: 366.25
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-Pyrimidinamine, N-(3-chlorophenyl)-4-[1-(2-methoxyethyl)-1H-imidazol-5-yl]-, monohydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: 2-Pyrimidinamine, N-(3-chlorophenyl)-4-[1-(2-methoxyethyl)-1H-imidazol-5-yl]-, monohydrochloride(403791-08-2)
EPA Substance Registry System: 2-Pyrimidinamine, N-(3-chlorophenyl)-4-[1-(2-methoxyethyl)-1H-imidazol-5-yl]-, monohydrochloride(403791-08-2)

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: 403791-08-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 403791-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,3,7,9 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 403791-08:
(8*4)+(7*0)+(6*3)+(5*7)+(4*9)+(3*1)+(2*0)+(1*8)=132
132 % 10 = 2
So 403791-08-2 is a valid CAS Registry Number.

403791-08-2Upstream product

403791-08-2Downstream Products

403791-08-2Relevant academic research and scientific papers

Imidazolo-5-YL-2anilino-pyrimidines as agents for the inhibition of the cell proliffration

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Page/Page column 17, (2010/02/05)

Compounds of the formula (I): wherein R1, R2, R3, R4, R5, R6, p, q, and n are as defined within and a pharmaceutically acceptable salts and in vivo hydrolysable esters are described. Also described are processes for their preparation and their use as medicaments, particularly medicaments for producing a cell cycle inhibitory (anti-cell-proliferation) effect in a warm-blooded animal, such as man.

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