7190-58-1 Usage
Description
(3-OXO-BUTYRYL)-CARBAMIC ACID ETHYL ESTER is a chemical compound with the molecular formula C7H11NO4. It is an ethyl ester of (3-oxobutyl)carbamic acid, which is a derivative of carbamic acid. This colorless to light yellow liquid with a faint odor is miscible in water and many organic solvents.
Used in Pharmaceutical Industry:
(3-OXO-BUTYRYL)-CARBAMIC ACID ETHYL ESTER is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the formation of complex drug molecules.
Used in Agrochemical Industry:
(3-OXO-BUTYRYL)-CARBAMIC ACID ETHYL ESTER is used as a precursor in the preparation of various pesticide and fungicide products, playing a crucial role in the development of effective crop protection agents.
Used in Organic Synthesis:
(3-OXO-BUTYRYL)-CARBAMIC ACID ETHYL ESTER is used as a solvent or reagent in organic synthesis, facilitating a range of chemical reactions due to its miscibility with water and many organic solvents.
Check Digit Verification of cas no
The CAS Registry Mumber 7190-58-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,9 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7190-58:
(6*7)+(5*1)+(4*9)+(3*0)+(2*5)+(1*8)=101
101 % 10 = 1
So 7190-58-1 is a valid CAS Registry Number.
7190-58-1Relevant articles and documents
Heterocyclic Transformations. Part 3. Thiolate Ion-induced Transformations of 6-Methyl-1,3-oxazine-2,4(3H)-diones to 3-(Alkyl/arylthio)but-2-enamides
Kumar, Subodh,Chimni, Swapandeep Singh,Singh, Harjit
, p. 1391 - 1395 (2007/10/02)
Thiolate ions generated under phase-transfer catalytic conditions react exclusively at C-6 of 3-alkyl-6-methyl-1,3-oxazine-2,4(3H)-diones to give (E)- and (Z)-3-(alkylthio)but-2-enamides.With binucleophiles having at least one thiol group, the E+Z thiobutenamides are initially formed and their further transformation depends on the nature on the second nucleophile.The bulk of the N-3 substituent of the oxazine and the thiol exercise steric control on the rate and mode of the reaction.
