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10457-86-0

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10457-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10457-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,5 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10457-86:
(7*1)+(6*0)+(5*4)+(4*5)+(3*7)+(2*8)+(1*6)=90
90 % 10 = 0
So 10457-86-0 is a valid CAS Registry Number.

10457-86-0SDS

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 butyl 1,1-dimethyl-3,6-dihydro-2H-pyridin-1-ium-5-carboxylate,iodide

1.2 Other means of identification

Product number -
Other names butyl 1,1-dimethyl-3,6-dihydro-2H-pyridin-1-ium-5-carboxylate iodide

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:10457-86-0 SDS

10457-86-0Downstream Products

10457-86-0Relevant articles and documents

Muscarinic properties of compounds related to arecaidine propargyl ester

Tumiatti, Vincenzo,Wehrle, Jahn,Hildebrandt, Caren,Moser, Ulrich,Dannhardt, Gerd,Mutschler, Ernst,Lambrecht, Guenter

, p. 11 - 15 (2007/10/03)

A series of new analogues of the arecaidine propargyl ester (CAS 35516- 99-5, APE, la) with alcohols consisting of 4 or 5 carbon atoms were investigated at muscarinic receptor subtypes. The muscarinic activity of the quaternary and tertiary salts of the APE-related compounds were assayed on the isolated guinea-pig ileum (M3 receptor subtype) and guinea-pig left atria (M2 receptor subtype) as well as on rabbit isolated vas deferens (M1 receptor subtype). The structural variations made in the APE molecule, replacing the triple bond in the ester side chain with structures such as double bond, an allene moiety, a single bond, a cyclopropyl group or two triple bonds should alter the selectivity and potency in favour of the M2 subtype. Enhanced, though modest, selectivity for M2 receptors was achieved with the 2-butynyl ester 2a. The other structural variations resulted in a loss of potency, but not necessarily of efficacy.

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