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Benzamide, 4-amino-N-1-azabicyclo[2.2.2]oct-4-yl-5-chloro-2-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106792-80-7

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106792-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106792-80-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,7,9 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 106792-80:
(8*1)+(7*0)+(6*6)+(5*7)+(4*9)+(3*2)+(2*8)+(1*0)=137
137 % 10 = 7
So 106792-80-7 is a valid CAS Registry Number.

106792-80-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-N-(1-azabicyclo[2.2.2]oct-4-yl)-5-chloro-2-methoxybenzamide

1.2 Other means of identification

Product number -
Other names 4-Amino-N-(1-aza-bicyclo[2.2.2]oct-4-yl)-5-chloro-2-methoxy-benzamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:106792-80-7 SDS

106792-80-7Downstream Products

106792-80-7Relevant academic research and scientific papers

Substituted Benzamides with Conformationally Restricted Side Chains. 5. Azabicyclo Derivatives as 5-HT4 Receptor Agonists and Gastric Motility Stimulants

King, Frank D.,Hadley, Michael S.,Joiner, Karen T.,Martin, Roger T.,Sanger, Gareth J.,et al.

, p. 683 - 689 (2007/10/02)

The syntheses of benzamides containing azabicyclo side chains and their 5-HT4 receptor agonist and 5-HT3 receptor antagonist properties are described.These compounds were designed to mimic higher energy conformations of quinol

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