Cas 849470-71-9,5-Pyrimidinecarboxylic acid, 4-(4-fluorophenyl)-6-(1-methylethyl)-2-[(1-methyl-1H-pyrazol-5-yl)amino]- , ethyl ester

849470-71-9

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Basic information

Product Name: 5-Pyrimidinecarboxylic acid, 4-(4-fluorophenyl)-6-(1-methylethyl)-2-[(1-methyl-1H-pyrazol-5-yl)amino]- , ethyl ester
Synonyms:
CAS NO:849470-71-9
Molecular Formula: C20H22FN5O2
Molecular Weight: 383.425
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: 5-Pyrimidinecarboxylic acid, 4-(4-fluorophenyl)-6-(1-methylethyl)-2-[(1-methyl-1H-pyrazol-5-yl)amino]- , ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 5-Pyrimidinecarboxylic acid, 4-(4-fluorophenyl)-6-(1-methylethyl)-2-[(1-methyl-1H-pyrazol-5-yl)amino]- , ethyl ester(849470-71-9)
EPA Substance Registry System: 5-Pyrimidinecarboxylic acid, 4-(4-fluorophenyl)-6-(1-methylethyl)-2-[(1-methyl-1H-pyrazol-5-yl)amino]- , ethyl ester(849470-71-9)

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: 849470-71-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 849470-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,4,7 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 849470-71:
(8*8)+(7*4)+(6*9)+(5*4)+(4*7)+(3*0)+(2*7)+(1*1)=209
209 % 10 = 9
So 849470-71-9 is a valid CAS Registry Number.

849470-71-9Upstream product

849470-71-9Downstream Products

849470-74-2 C₂₈H₃₀FN₅O₃

849470-71-9Relevant academic research and scientific papers

PYRIMIDINE AND PYRIDINE DERIVATIVES USEFUL AS HMG-COA REDUCTASE INHIBITORS AND METHOD OF PREPARATION THEREOF

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Page/Page column 60-61, (2010/02/11)

Compounds are provided having the following structure which are HMG CoA reductase inhibitors and thus are active in inhibiting cholesterol biosynthesis, modulating blood serum lipids, for example, lowering LDL cholesterol and/or increasing HDL cholesterol

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