152009-44-4 Usage
General Description
Ethyl ThioMorpholine-2-carboxylate is a chemical compound commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. It is a thiomorpholine derivative, which is a class of heterocyclic organic compounds. This chemical possesses a similar structure to morpholine, and the addition of the thiol group provides it with unique properties and reactivity. Ethyl ThioMorpholine-2-carboxylate is used in the production of various drugs, including antifungal and antibacterial agents, as well as in the development of crop protection products. Its versatility and utility make it a valuable and important compound in the field of synthetic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 152009-44-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,0,0 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 152009-44:
(8*1)+(7*5)+(6*2)+(5*0)+(4*0)+(3*9)+(2*4)+(1*4)=94
94 % 10 = 4
So 152009-44-4 is a valid CAS Registry Number.
152009-44-4Relevant articles and documents
Preparation method of N-hydro/N-alkylated thiomorpholin-2-carboxylic acid/carboxylate compound
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Paragraph 0073; 0075; 0077, (2019/04/17)
The invention relates to a preparation method of a N-hydro/N-alkylated thiomorpholin-2-carboxylic acid/carboxylate compound. The method includes: subjecting a compound shown as formula (II) to reaction with R3COOH and alkali-metal borohydrides to obtain the N-hydro/N-alkylated thiomorpholin-2-carboxylic acid/carboxylate compound shown as formula (I), wherein R1 is selected from hydrogen and substituted or non-substituted alkyl group, R2 is selected from hydrogen and substituted or non-substituted alkyl group, and R3 is selected from hydrogen and substituted or non-substituted alkyl group. Thepreparation method of the N-hydro/N-alkylated thiomorpholin-2-carboxylic acid/carboxylate compound has a short synthetic route; the target product can be acquired just through two steps; reaction materials are easy to attain; the cost is low; the preparation method is suitable for large-scale preparation, and is high in yield, up to 34.3% to 60.7%.
