Cas 1026599-48-3,{1-[(1-benzyl-3-benzylcarbamoyl-3,3-difluoro-2-oxo-propylcarbamoyl)-methyl]-6-oxo-2-<i>m</i>-tolyl-1,6-dihydro-pyrimidin-5-yl}-carbamic acid benzyl ester

1026599-48-3

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Basic information

Product Name: {1-[(1-benzyl-3-benzylcarbamoyl-3,3-difluoro-2-oxo-propylcarbamoyl)-methyl]-6-oxo-2-m-tolyl-1,6-dihydro-pyrimidin-5-yl}-carbamic acid benzyl ester
Synonyms: {1-[(1-benzyl-3-benzylcarbamoyl-3,3-difluoro-2-oxo-propylcarbamoyl)-methyl]-6-oxo-2-m-tolyl-1,6-dihydro-pyrimidin-5-yl}-carbamic acid benzyl ester
CAS NO:1026599-48-3
Molecular Formula:
Molecular Weight: 707.734
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]-6-oxo-2-m-tolyl-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]-6-oxo-2-m-tolyl-1,6-dihydro-pyrimidin-5-yl}-carbamic acid benzyl ester(1026599-48-3)
EPA Substance Registry System: {1-[(1-benzyl-3-benzylcarbamoyl-3,3-difluoro-2-oxo-propylcarbamoyl)-methyl]-6-oxo-2-m-tolyl-1,6-dihydro-pyrimidin-5-yl}-carbamic acid benzyl ester(1026599-48-3)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1026599-48-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1026599-48-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,6,5,9 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1026599-48:
(9*1)+(8*0)+(7*2)+(6*6)+(5*5)+(4*9)+(3*9)+(2*4)+(1*8)=163
163 % 10 = 3
So 1026599-48-3 is a valid CAS Registry Number.

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1026599-48-3Relevant 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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