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Atropine N-oxide hydrochloride is a chemical compound derived from atropine, an alkaloid found in the deadly nightshade plant. It is a white crystalline powder with the chemical formula C17H22ClNO3 and a molecular weight of 327.81 g/mol. ATROPINE N-OXIDE HYDROCHLORIDE is used as an intermediate in the synthesis of various drugs, including atropine sulfate, which is a muscarinic antagonist used to treat conditions like organophosphate poisoning, bradycardia, and to reduce secretions during surgery. Atropine N-oxide hydrochloride is also employed in research to study the pharmacological properties of atropine and its derivatives. It is important to note that handling ATROPINE N-OXIDE HYDROCHLORIDE requires appropriate safety measures due to its potential toxicity.

4574-60-1

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4574-60-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4574-60-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,7 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4574-60:
(6*4)+(5*5)+(4*7)+(3*4)+(2*6)+(1*0)=101
101 % 10 = 1
So 4574-60-1 is a valid CAS Registry Number.
InChI:InChI=1/C17H21NO3.ClH/c1-12(13-6-4-3-5-7-13)17(19)21-16-10-14-8-9-15(11-16)18(14,2)20;/h3-7,14-16H,1,8-11H2,2H3;1H/t14-,15+,16-,18-;

4574-60-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ATROPINE N-OXIDE HYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names DL-tropic acid-(8-oxy-tropane-3endo-yl ester),hydrochloride

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:4574-60-1 SDS

4574-60-1Upstream product

4574-60-1Relevant academic research and scientific papers

Utility of iron nanoparticles and a solution-phase iron species for the: N-demethylation of alkaloids

Awalt, Jon Kyle,Lam, Raymond,Kellam, Barrie,Graham, Bim,Scammells, Peter J.,Singer, Robert D.

supporting information, p. 2587 - 2594 (2017/07/17)

The N-demethylation of selected N-methylalkaloids using a modified Polonovski reaction can be accomplished using a novel green methodology employing nanoscale zero-valent iron, nZVI, in isopropanol. Use of nZVI promotes a much faster conversion to N-demethylated products due to much higher surface area on the metal surface as shown by SEM analysis. Rates of conversion can be further enhanced using catalytic quantities of the solubilised iron(0) species triiron dodecacarbonyl, Fe3(CO)12.

N-Demethylation of N-methyl alkaloids with ferrocene

Kok, Gaik B.,Scammells, Peter J.

supporting information; experimental part, p. 4499 - 4502 (2010/09/15)

Under Polonovski-type conditions, ferrocene has been found to be a convenient and efficient catalyst for the N-demethylation of a number of N-methyl alkaloids such as opiates and tropanes. By judicious choice of solvent, good yields have been obtained for dextromethorphan, codeine methyl ether, and thebaine. The current methodology is also successful for the N-demethylation of morphine, oripavine, and tropane alkaloids, producing the corresponding N-nor compounds in reasonable yields. Key pharmaceutical intermediates such oxycodone and oxymorphone are also readily N-demethylated using this approach.

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