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4438-22-6

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4438-22-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4438-22-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,3 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4438-22:
(6*4)+(5*4)+(4*3)+(3*8)+(2*2)+(1*2)=86
86 % 10 = 6
So 4438-22-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H23NO4/c1-18(21)13-7-8-14(18)10-15(9-13)22-17(20)16(11-19)12-5-3-2-4-6-12/h2-6,13-16,19H,7-11H2,1H3/t13-,14+,15+,16?,18?

4438-22-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-Azabicyclo[3.2.1]octan-3.α.-ol, 8-methyl-, 8-oxide, tropate

1.2 Other means of identification

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

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:4438-22-6 SDS

4438-22-6Downstream Products

4438-22-6Relevant articles and documents

Kinetic and polarographic study on atropine N-oxide: its obtaining and polarographic reduction

Dubenska, Liliya,Dushna, Olha,Blazheyevskiy, Mykola,Pysarevska, Solomiya,Klymiuk, Iryna

, p. 4147 - 4155 (2021/04/29)

The work presents the obtaining of atropine N-oxide using various peroxyacids (organic monoperoxyacid, diperoxyacids and inorganic peroxyacids). The kinetics of atropine oxidation with various oxidants, for example Oxone, m-chloroperoxybenzoic acid, diperoxysebasic acid and diperoxyazelaic acid, was studied. The optimal conditions for obtaining of atropine N-oxide (oxidation duration, pH) are given in the work. It was established that the best oxidant was potassium peroxymonosulfate, since 100% yield of atropine N-oxide was achieved within 15?min. In this work, we showed that the oxidation reaction of atropine to N-oxide was a second-order reaction. The rate constants of these reactions were established. The electrochemical behavior of atropine N-oxide obtained using potassium peroxymonosulfate and m-chloroperoxybenzoic acid on a mercury dropping electrode was investigated. Atropine N-oxide was reduced forming two peaks. Each reduction peak involved 1 electron and 1 proton.

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