Cas 1034495-87-8,N-(2-t-butoxycarbonylamino-5-methoxyphenyl)-4-[1-(2-dimethylaminoethyl)-3-(indan-5-yl)ureidomethyl]benzamide

1034495-87-8

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Basic information

Product Name: N-(2-t-butoxycarbonylamino-5-methoxyphenyl)-4-[1-(2-dimethylaminoethyl)-3-(indan-5-yl)ureidomethyl]benzamide
Synonyms: N-(2-t-butoxycarbonylamino-5-methoxyphenyl)-4-[1-(2-dimethylaminoethyl)-3-(indan-5-yl)ureidomethyl]benzamide
CAS NO:1034495-87-8
Molecular Formula:
Molecular Weight: 601.746
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: N-(2-t-butoxycarbonylamino-5-methoxyphenyl)-4-[1-(2-dimethylaminoethyl)-3-(indan-5-yl)ureidomethyl]benzamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(2-t-butoxycarbonylamino-5-methoxyphenyl)-4-[1-(2-dimethylaminoethyl)-3-(indan-5-yl)ureidomethyl]benzamide(1034495-87-8)
EPA Substance Registry System: N-(2-t-butoxycarbonylamino-5-methoxyphenyl)-4-[1-(2-dimethylaminoethyl)-3-(indan-5-yl)ureidomethyl]benzamide(1034495-87-8)

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: 1034495-87-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1034495-87-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,4,4,9 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1034495-87:
(9*1)+(8*0)+(7*3)+(6*4)+(5*4)+(4*9)+(3*5)+(2*8)+(1*7)=148
148 % 10 = 8
So 1034495-87-8 is a valid CAS Registry Number.

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1034495-87-8Relevant academic research and scientific papers

NOVEL N-(2-AMINOPHENYL)BENZAMIDE DERIVATIVE HAVING AN UREA STRUCTURE

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Page/Page column 78, (2009/10/18)

The present invention relates to a study on the sy nthesis of a novel N-(2-aminophenyl)benzamide derivativ e having an urea structure and represented by the genera l formula (1); and the utilization of a pharmacological effect of the derivative. A compoun

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