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133342-59-3

133342-59-3

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133342-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133342-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,3,4 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 133342-59:
(8*1)+(7*3)+(6*3)+(5*3)+(4*4)+(3*2)+(2*5)+(1*9)=103
103 % 10 = 3
So 133342-59-3 is a valid CAS Registry Number.
InChI:InChI=1/C21H27NO3/c1-3-22(14-16-23)15-17-25-20(24)21(2,18-10-6-4-7-11-18)19-12-8-5-9-13-19/h4-13,23H,3,14-17H2,1-2H3

133342-59-3SDS

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 2-[ethyl(2-hydroxyethyl)amino]ethyl 2,2-diphenylpropanoate

1.2 Other means of identification

Product number -
Other names -

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:133342-59-3 SDS

133342-59-3Downstream Products

133342-59-3Relevant articles and documents

Synthesis and antimuscarinic activity of 2-[N-(ethyl)-(N-β- hydroxyethyl)]aminoethyl 2,2-diphenylpropionate, a metabolite of aprophen

Brown,Leader,Phillips,Smejkal,Gordon,Chiang

, p. 563 - 564 (2007/10/02)

The preparation of 2-[N-(ethyl)-(N-β-hydroxyethyl)]aminoethyl 2,2- diphenylpropionate (1), a metabolite of aprophen [2-diethylaminoethyl 2,2- diphenylpropionate], is described. Hydrolysis of [2-(2- chloroethyl)ethylamino]ethyl acetate hydrochloride (2) in a basic solution, followed by acidic pH adjustment, gave the ethylcholineaziridinium ion (3) that upon treatment with 2,2-diphenylpropionic acid produced 1 in a 56% yield. Synthetic 1 was found to possess antimuscarinic activities, but was ~10-fold less potent than the parent compound aprophen.

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