Cas 1027661-57-9,[(2-{3-[4-(5-chloro-pyrimidin-2-yloxy)-3-trifluoromethyl-phenyl]-ureidocarbonyl}-phenylcarbamoyl)-methyl]-carbamic acid <i>tert</i>-butyl ester

1027661-57-9

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Basic information

Product Name: [(2-{3-[4-(5-chloro-pyrimidin-2-yloxy)-3-trifluoromethyl-phenyl]-ureidocarbonyl}-phenylcarbamoyl)-methyl]-carbamic acid tert-butyl ester
Synonyms:
CAS NO:1027661-57-9
Molecular Formula:
Molecular Weight: 608.961
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-{3-[4-(5-chloro-pyrimidin-2-yloxy)-3-trifluoromethyl-phenyl]-ureidocarbonyl}-phenylcarbamoyl)-methyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(2-{3-[4-(5-chloro-pyrimidin-2-yloxy)-3-trifluoromethyl-phenyl]-ureidocarbonyl}-phenylcarbamoyl)-methyl]-carbamic acid tert-butyl ester(1027661-57-9)
EPA Substance Registry System: [(2-{3-[4-(5-chloro-pyrimidin-2-yloxy)-3-trifluoromethyl-phenyl]-ureidocarbonyl}-phenylcarbamoyl)-methyl]-carbamic acid tert-butyl ester(1027661-57-9)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1027661-57-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1027661-57-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,6,6 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1027661-57:
(9*1)+(8*0)+(7*2)+(6*7)+(5*6)+(4*6)+(3*1)+(2*5)+(1*7)=139
139 % 10 = 9
So 1027661-57-9 is a valid CAS Registry Number.

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1027661-57-9Relevant academic research and scientific papers

Synthesis and antitumor activities of water-soluble benzoylphenylureas

Okada, Hiroshi,Kato, Masanari,Koyanagi, Tohru,Mizuno, Kazuhiko

, p. 430 - 433 (2007/10/03)

Water-soluble benzoylphenylurea derivatives were synthesized as candidate prodrugs and their antitumor activities were examined in vivo against P388 leukemia. Some of the prodrugs were highly soluble in water and showed good antitumor activities against P388 leukemia cells in mice when injected intravenously.

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