29818-16-4 Usage
Molecular weight
222.27 g/mol
Functional groups
methyl group, ethyl group, acetoacetate group, allyl ester group
Polarity
moderate to high (due to presence of ester and carbonyl groups)
Solubility
soluble in organic solvents (e.g. acetone, ethanol, dichloromethane) but not water
Reactivity
versatile reagent in organic synthesis, useful intermediate for the synthesis of various organic compounds
Synthesis
member of the acetoacetate family of compounds, used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 29818-16-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,1 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 29818-16:
(7*2)+(6*9)+(5*8)+(4*1)+(3*8)+(2*1)+(1*6)=144
144 % 10 = 4
So 29818-16-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O5/c1-4-9(12)14-6-8(3)15-10(13)5-7(2)11/h4,8H,1,5-6H2,2-3H3
29818-16-4Relevant articles and documents
Diastereoselective synthesis of bis(3,5)pyrazolophanes by sequential inter- and intramolecular cycloadditions of homochiral nitrilimines
Broggini, Gianluigi,Molteni, Giorgio,Pilati, Tullio
, p. 1975 - 1983 (2007/10/03)
Starting from ethyl (S)-lactate as the chiral unit, we have developed the synthesis of the enantiopure bis(3,5)pyrazolophanes 9 and 19 by means of sequential inter- and intramolecular cycloadditions of nitrilimine intermediates. Copyright (C) 2000 Elsevie
