Cas 139632-52-3,Benzamide, N-[[(8-methyl-8-azabicyclo[3.2.1]oct-3-yl)amino]carbonyl]-2-(3-methylbut oxy)-, endo-

139632-52-3

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Basic information

Product Name: Benzamide, N-[[(8-methyl-8-azabicyclo[3.2.1]oct-3-yl)amino]carbonyl]-2-(3-methylbut oxy)-, endo-
Synonyms:
CAS NO:139632-52-3
Molecular Formula: C21H31N3O3
Molecular Weight: 373.495
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: Benzamide, N-[[(8-methyl-8-azabicyclo[3.2.1]oct-3-yl)amino]carbonyl]-2-(3-methylbut oxy)-, endo-(CAS DataBase Reference)
NIST Chemistry Reference: Benzamide, N-[[(8-methyl-8-azabicyclo[3.2.1]oct-3-yl)amino]carbonyl]-2-(3-methylbut oxy)-, endo-(139632-52-3)
EPA Substance Registry System: Benzamide, N-[[(8-methyl-8-azabicyclo[3.2.1]oct-3-yl)amino]carbonyl]-2-(3-methylbut oxy)-, endo-(139632-52-3)

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: 139632-52-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 139632-52-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,6,3 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 139632-52:
(8*1)+(7*3)+(6*9)+(5*6)+(4*3)+(3*2)+(2*5)+(1*2)=143
143 % 10 = 3
So 139632-52-3 is a valid CAS Registry Number.

139632-52-3Upstream product

139632-52-3Downstream Products

139632-52-3Relevant academic research and scientific papers

Novel antagonists of the 5-HT3 receptor. Synthesis and structure-activity relationships of (2-alkoxybenzoyl)ureas

Bradley,Ward,White,Coleman,Taylor,Rhodes

, p. 1515 - 1520 (2007/10/02)

A series of benzoylureas derived from bicycle amines were prepared and evaluated for 5-HT3 antagonist activity on the rat isolated vagus nerve. From among these compounds, those analogues which were ortho substituted by an alkoxy group on the b

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