Cas 1027248-69-6,[1-[(1-benzyl-3-benzylcarbamoyl-3,3-difluoro-2-oxo-propylcarbamoyl)-methyl]-2-(3-fluoro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-5-yl]-carbamic acid benzyl ester

1027248-69-6

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Product Name: [1-[(1-benzyl-3-benzylcarbamoyl-3,3-difluoro-2-oxo-propylcarbamoyl)-methyl]-2-(3-fluoro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-5-yl]-carbamic acid benzyl ester
Synonyms: [1-[(1-benzyl-3-benzylcarbamoyl-3,3-difluoro-2-oxo-propylcarbamoyl)-methyl]-2-(3-fluoro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-5-yl]-carbamic acid benzyl ester
CAS NO:1027248-69-6
Molecular Formula:
Molecular Weight: 711.697
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: [1-[(1-benzyl-3-benzylcarbamoyl-3,3-difluoro-2-oxo-propylcarbamoyl)-methyl]-2-(3-fluoro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-5-yl]-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [1-[(1-benzyl-3-benzylcarbamoyl-3,3-difluoro-2-oxo-propylcarbamoyl)-methyl]-2-(3-fluoro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-5-yl]-carbamic acid benzyl ester(1027248-69-6)
EPA Substance Registry System: [1-[(1-benzyl-3-benzylcarbamoyl-3,3-difluoro-2-oxo-propylcarbamoyl)-methyl]-2-(3-fluoro-phenyl)-6-oxo-1,6-dihydro-pyrimidin-5-yl]-carbamic acid benzyl ester(1027248-69-6)

Safety Data

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
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Hazardous Substances Data: 1027248-69-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1027248-69-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,2,4 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1027248-69:
(9*1)+(8*0)+(7*2)+(6*7)+(5*2)+(4*4)+(3*8)+(2*6)+(1*9)=136
136 % 10 = 6
So 1027248-69-6 is a valid CAS Registry Number.

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1027248-69-6Relevant academic research and scientific papers

Synthesis, structure - Activity relationships, and pharmacokinetic profiles of nonpeptidic difluoromethylene ketones as novel inhibitors of human chymase

Akahoshi,Ashimori,Sakashita,Yoshimura,Eda,Imada,Nakajima,Mitsutomi,Kuwahara,Ohtsuka,Fukaya,Miyazaki,Nakamura

, p. 1297 - 1304 (2007/10/03)

Potent human chymase inhibitors with high enzymatic selectivity and satisfactory metabolic stability were obtained by replacing the Val-Pro (P3-P2) dipeptide portion of the previously described inhibitor 1 with a nonpeptidic pyrimidi

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