Cas 1615693-71-4,4-(3-ethoxycarbonyl-2-methylguanidino)-N-(4-(3-ethoxycarbonyl-2-methylguanidino)phenyl)benzamide

1615693-71-4

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Basic information

Product Name: 4-(3-ethoxycarbonyl-2-methylguanidino)-N-(4-(3-ethoxycarbonyl-2-methylguanidino)phenyl)benzamide
Synonyms: 4-(3-ethoxycarbonyl-2-methylguanidino)-N-(4-(3-ethoxycarbonyl-2-methylguanidino)phenyl)benzamide
CAS NO:1615693-71-4
Molecular Formula:
Molecular Weight: 483.527
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: 4-(3-ethoxycarbonyl-2-methylguanidino)-N-(4-(3-ethoxycarbonyl-2-methylguanidino)phenyl)benzamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-(3-ethoxycarbonyl-2-methylguanidino)-N-(4-(3-ethoxycarbonyl-2-methylguanidino)phenyl)benzamide(1615693-71-4)
EPA Substance Registry System: 4-(3-ethoxycarbonyl-2-methylguanidino)-N-(4-(3-ethoxycarbonyl-2-methylguanidino)phenyl)benzamide(1615693-71-4)

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: 1615693-71-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1615693-71-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,5,6,9 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1615693-71:
(9*1)+(8*6)+(7*1)+(6*5)+(5*6)+(4*9)+(3*3)+(2*7)+(1*1)=184
184 % 10 = 4
So 1615693-71-4 is a valid CAS Registry Number.

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1615693-71-4Relevant academic research and scientific papers

Antiprotozoal activity and DNA binding of N-substituted N-phenylbenzamide and 1,3-diphenylurea bisguanidines

Ríos Martínez, Carlos H.,Lagartera, Laura,Kaiser, Marcel,Dardonville, Christophe

, p. 481 - 491 (2014/06/09)

Two series of N-alkyl, N-alkoxy, and N-hydroxy bisguanidines derived from the N-phenylbenzamide and 1,3-diphenylurea scaffolds were synthesised in three steps from the corresponding 4-amino-N-(4-aminophenyl)benzamide and 1,3-bis(4-aminophenyl)urea, respec

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