16798-45-1 Usage
General Description
Diethyl benzamidomalonate is a synthetic chemical compound used in organic synthesis as an intermediate for the production of pharmaceuticals and other specialty chemicals. It is a white to off-white crystalline powder that is soluble in organic solvents like ethanol and acetone. Diethyl benzamidomalonate is commonly used in the pharmaceutical industry for the synthesis of various types of drugs, particularly those designed to treat cardiovascular and central nervous system disorders. It is also used as a building block in the production of agrochemicals and other specialty chemicals. The compound is typically handled and stored under controlled conditions to prevent degradation and ensure its stability.
Check Digit Verification of cas no
The CAS Registry Mumber 16798-45-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,9 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16798-45:
(7*1)+(6*6)+(5*7)+(4*9)+(3*8)+(2*4)+(1*5)=151
151 % 10 = 1
So 16798-45-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H17NO5/c1-3-19-13(17)11(14(18)20-4-2)12(16)15-10-8-6-5-7-9-10/h5-9,11H,3-4H2,1-2H3,(H,15,16)
16798-45-1Relevant articles and documents
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Kociolek,K.,Leplawy,M.T.
, p. 778 - 780 (1977)
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Indium-Mediated Blaise-Type Reaction of Bromomalonates with Nitriles and Isocyanates
Babaoglu, Emre,Harms, Klaus,Hilt, Gerhard
supporting information, p. 1820 - 1823 (2016/07/16)
The indium-mediated Blaise-type reaction of bromomalonates with nitriles and isocyanates is described. The choice of the solvent is crucial for the successful reaction; the dependency on dichloromethane proved to be nonplussed. The reaction with nitriles
The chemistry of 5-oxodihydroisoxazoles V: The photolysis of 2-phenylisoxazol-5(2H)-one ln alcohols
Ang, Kiah H.,Prager, Rolf H.
, p. 9073 - 9084 (2007/10/02)
Ethyl 5-oxo-2-phenyl-2,5-dihydroisoxazole-4-carboxylate (1) has been photolysed in methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, t-butyl alcohol, allyl alcohol and propargyl alcohol, and the products characterised. Two types of photo products are formed: methanetricarboxylic acid derivatives resulting from alcohol capture of the first formed ketene, and 2-alkoxy-3-phenylaminoacrylates, formed by capture, by the alcohol, of the imino-carbene arising from (1) by loss of carbon dioxide.
