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63144-70-7

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63144-70-7 Usage

Functional groups

acetyl group, benzyl group, amino group, ethyl group

Ester linkage

connects the phenyl and acetyl groups

Potential applications

organic synthesis, pharmaceuticals, materials science
Further research needed to fully understand properties and potential uses

Check Digit Verification of cas no

The CAS Registry Mumber 63144-70-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,4 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63144-70:
(7*6)+(6*3)+(5*1)+(4*4)+(3*4)+(2*7)+(1*0)=107
107 % 10 = 7
So 63144-70-7 is a valid CAS Registry Number.

63144-70-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-[2-[acetyl-[(3-acetyloxyphenyl)methyl]amino]ethyl]phenyl] acetate

1.2 Other means of identification

Product number -
Other names 4-(2-{acetyl[3-(acetyloxy)benzyl]amino}ethyl)phenyl acetate

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:63144-70-7 SDS

63144-70-7Relevant articles and documents

Chromium-Salen Complex/Nitroxyl Radical Cooperative Catalysis: A Combination for Aerobic Intramolecular Dearomative Coupling of Phenols

Nagasawa, Shota,Fujiki, Shogo,Sasano, Yusuke,Iwabuchi, Yoshiharu

, p. 6952 - 6968 (2021/05/29)

We describe an aerobic intramolecular dearomative coupling reaction of tethered phenols using a catalytic system consisting of a chromium-salen (Cr-salen) complex combined with a nitroxyl radical. This novel catalytic system enables formation of various spirocyclic dienone products including those unable to be accessed by previously reported methods efficiently under mild reaction conditions.

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