84099-74-1 Usage
Description
Ethyl 3-oxothiomorpholine-2-carboxylate is a chemical compound with the molecular formula C7H11NO4S. It is a derivative of thiomorpholine, a heterocyclic amine containing a sulfur atom in the six-membered ring. Its unique ring structure and functional groups make it useful in various organic reactions and as an intermediate in the synthesis of pharmaceuticals and agrochemicals.
Uses
Used in Pharmaceutical Industry:
Ethyl 3-oxothiomorpholine-2-carboxylate is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of active pharmaceutical ingredients.
Used in Agrochemical Industry:
Ethyl 3-oxothiomorpholine-2-carboxylate is used as an intermediate in the synthesis of agrochemicals, playing a role in the production of various agricultural chemicals.
Used in Organic Reactions:
Ethyl 3-oxothiomorpholine-2-carboxylate is used in various organic reactions due to its unique ring structure and functional groups, which allow it to participate in a wide range of chemical processes.
Used in Drug Development:
Ethyl 3-oxothiomorpholine-2-carboxylate has potential applications in the development of new drugs and chemicals, as its properties can be harnessed to create novel therapeutic agents and chemical compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 84099-74-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,0,9 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 84099-74:
(7*8)+(6*4)+(5*0)+(4*9)+(3*9)+(2*7)+(1*4)=161
161 % 10 = 1
So 84099-74-1 is a valid CAS Registry Number.
84099-74-1Relevant articles and documents
Preparation of 2-Amino-4(3H)-oxopyrimidothiazines (5-Thiapterins) and Their Evaluation as Cofactors for Phenylalanine Hydroxylase
Henrie, Robert N.,Lazarus, Robert A.,Benkovic, Stephen J.
, p. 559 - 563 (2007/10/02)
Reaction of diethyl chloromalonate with β-mercapto amines, 9, gave 1,4-thiazin-3-ones, 10, which were alkylated exclusively at the lactam oxygen with triethyloxonium tetrafluoroborate and subsequently condensed with guanidine to give the first reported 5-
