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20284-85-9

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20284-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20284-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,8 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20284-85:
(7*2)+(6*0)+(5*2)+(4*8)+(3*4)+(2*8)+(1*5)=89
89 % 10 = 9
So 20284-85-9 is a valid CAS Registry Number.

20284-85-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-aminoethyl)-phenyl acetate

1.2 Other means of identification

Product number -
Other names 4-(2-aminoethyl)phenylacetate

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:20284-85-9 SDS

20284-85-9Relevant academic research and scientific papers

The use of immobilized crown ethers as in-situ N-protecting groups in organic synthesis and their application under continuous flow

Wild, Gareth. P.,Wiles, Charlotte,Watts, Paul,Haswell, Stephen J.

, p. 1618 - 1629 (2009)

In addition to their high affinity for inorganic cations, crown ethers have been shown to efficiently sequester ammonium ions, forming a stable adduct via hydrogen bonding. Using this principle, several authors have reported the use of crown ethers as protecting groups for amines however to date, their widespread use has been somewhat precluded by the difficulties associated with removal of the crown ether from the resulting reaction mixture. In order to address this problem, we report the preparation of an immobilized 18-crown-6 ether derivative and its incorporation into a flow reactor, demonstrating the ability to use and recycle the reagent for the chemoselective O-acylation and alkylation of bifunctional compounds such as 4-(2-aminoethyl)phenol and 4-nitrophenol.

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