19520-88-8 Usage
General Description
2-[bis(phenylmethyl)amino]ethyl acetate, also known as benzylmethylaminoethyl acetate, is a chemical compound with the molecular formula C19H23NO2. It is a member of the acetate esters class and it is used as a raw material in the production of pharmaceuticals, agrochemicals, and fragrances. This chemical is a clear, colorless to pale yellow liquid with a faint odor, and it is soluble in organic solvents such as ethanol and acetone. 2-[bis(phenylmethyl)amino]ethyl acetate has potential risks associated with it, as it may cause skin and eye irritation, and it should be handled with care, following appropriate safety measures and regulations.
Check Digit Verification of cas no
The CAS Registry Mumber 19520-88-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,5,2 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19520-88:
(7*1)+(6*9)+(5*5)+(4*2)+(3*0)+(2*8)+(1*8)=118
118 % 10 = 8
So 19520-88-8 is a valid CAS Registry Number.
InChI:InChI=1/C18H21NO2/c1-16(20)21-13-12-19(14-17-8-4-2-5-9-17)15-18-10-6-3-7-11-18/h2-11H,12-15H2,1H3
19520-88-8Relevant articles and documents
KOt-Bu-promoted selective ring-opening N-alkylation of 2-oxazolines to access 2-aminoethyl acetates and N-substituted thiazolidinones
Li, Bin,Lin, Qiao,Zhang, Shiling
supporting information, p. 492 - 501 (2020/05/18)
An efficient and simple KOt-Bu-promoted selective ring-opening N-alkylation of 2-methyl-2-oxazoline or 2-(methylthio)-4,5-dihydrothiazole with benzyl halides under basic conditions is described for the first time. The method provides a convenient and practical pathway for the synthesis of versatile 2-aminoethyl acetates and N-substituted thiazolidinones with good functional group tolerance and selectivity. KOt-Bu not only plays an important role to promote this ring-opening N-alkylation, but also acts as an oxygen donor.
The N-(2-acetoxyethyl) group as a new photolabile protecting group
Cossy, Janine,Rakotoarisoa, Haja
, p. 2097 - 2099 (2007/10/03)
The N-(2-acetoxyethyl) group can be cleaved by a photoinduced single electron transfer to 4,4'-dimethoxybenzophenone. (C) 2000 Published by Elsevier Science Ltd.
