40797-71-5 Usage
Uses
Used in Pharmaceutical Industry:
N-[(morpholin-4-yl)carbonyl]morpholine-4-carboxamide is used as a building block in the synthesis of various drugs and bioactive compounds due to its versatile chemical structure and reactivity.
Used in Organic Synthesis:
As a versatile intermediate, N-[(morpholin-4-yl)carbonyl]morpholine-4-carboxamide is used in organic synthesis for the preparation of a wide range of chemical compounds.
Used as a Reagent in Chemical Reactions:
N-[(morpholin-4-yl)carbonyl]morpholine-4-carboxamide is utilized as a reagent in various chemical reactions, contributing to the formation of desired products.
Used in Metal Ion Complexation:
N-[(morpholin-4-yl)carbonyl]morpholine-4carboxamide is used for forming stable complexes with various metal ions, which can be beneficial in various applications, such as catalysis or the development of new materials.
Used in Antifungal Applications:
N-[(morpholin-4-yl)carbonyl]morpholine-4-carboxamide has been studied for its potential antifungal properties, making it a candidate for use in antifungal agents or treatments.
Used in Anticancer Research:
N-[(morpholin-4-yl)carbonyl]morpholine-4carboxamide's potential anticancer properties are being investigated, which could lead to its use in the development of new cancer therapies or treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 40797-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,7,9 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40797-71:
(7*4)+(6*0)+(5*7)+(4*9)+(3*7)+(2*7)+(1*1)=135
135 % 10 = 5
So 40797-71-5 is a valid CAS Registry Number.
40797-71-5Relevant academic research and scientific papers
Nitration of 2-substituted pyrimidine-4,6-diones, structure and reactivity of 5,5-gem-dinitropyrimidine-4,6-diones
Langlet, Abraham,Latypov, Nikolaj V.,Wellmar, Ulf,Bemm, Ulf,Goede, Patrick,Bergman, Jan,Romero, Ivan
, p. 7833 - 7838 (2007/10/03)
Nitration of some 2-substituted pyrimidine-4,6-diones in sulfuric acid was studied, which afforded previously unknown 5,5-gem-dinitropyrimidine-4,6-diones in high yields. The gem-dinitro products were easily attacked by nucleophiles with concomitant formation of gem-dinitroacetyl derivatives, which in turn could be further hydrolyzed to salts of dinitromethane and triureas.
Carbonyl Isocyanate Isothiocyanate
Bunnenberg, Rolf,Jochims, Johannes C.
, p. 2064 - 2074 (2007/10/02)
A synthesis of carbonyl isocyanate isothiocyanate (1) is described. 1 reacts with H2O, H2S, or HCl to give the thiadiazines 3, 6, and 14, resp.With one mol equivalent of alcohol the isothiocyanates 7 are obtained which form with further alcohol or amines compounds 8 - 10.With one mol equivalent of amine 1 gives the carbamoyl isothiocyanates 11 which form compounds 12 and 13 with further amine.Compound 1 can be chlorinated to carbonyl isocyanate isocyanide dichloride (18).Partial hydrolysis of 18 leads to carbamoyl isocyanide dichloride (19) yielding with aliphaticamines the stable carbamoyl carbodiimides 16.With alcohols 18 reacts to give the (dichloromethylene)allophanic esters 20.
