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19056-89-4

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19056-89-4 Usage

General Description

The chemical compound ((5-methyl-2-pyridinylamino)methylene)malonic acid diethyl ester, also known as Tryptorelin, is a diethyl ester of malonic acid bearing a 5-methyl-2-pyridinylaminomethylene group. It is a synthetic decapeptide agonist analogue of gonadotropin-releasing hormone (GnRH) that acts as a potent agonist at pituitary GnRH receptors. ((5-METHYL-2-PYRIDINYLAMINO)METHYLENE)MALONIC ACID DIETHYL ESTER is commonly used in medical research and clinical applications as a treatment for conditions related to hormone imbalances, such as prostate cancer and endometriosis. It functions by stimulating the release of gonadotropins, which can regulate the production and release of sex hormones.

Check Digit Verification of cas no

The CAS Registry Mumber 19056-89-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,5 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19056-89:
(7*1)+(6*9)+(5*0)+(4*5)+(3*6)+(2*8)+(1*9)=124
124 % 10 = 4
So 19056-89-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H18N2O4/c1-4-19-13(17)11(14(18)20-5-2)9-16-12-7-6-10(3)8-15-12/h6-9H,4-5H2,1-3H3,(H,15,16)

19056-89-4Relevant articles and documents

On the Regioselectivity of the Gould–Jacobs Reaction: Gas-Phase Versus Solution-Phase Thermolysis

Boese, A. Daniel,Dallinger, Doris,Darvas, Ferenc,Hartmann, Peter E.,Kappe, C. Oliver,Sipos, Gellért,Wernik, Michaela

, p. 7051 - 7061 (2020/11/30)

A detailed investigation of the regioselectivity in the thermal cyclization of (pyridyl)aminomethylenemalonates both in the gas- and solution phase is presented. Flash vacuum pyrolysis (FVP) as a gas-phase thermolysis technique is used to study the Gould–Jacobs reaction at temperatures between 450–650 °C, while different solution-phase heating techniques (reflux, microwave, and continuous flow) were employed at 260–350 °C. Depending on the position of the substituent in the pyridine moiety and the applied thermolysis technique, the regioselectivity of the cyclization can be controlled either in favor of the kinetic (pyridopyrimidinone) or the thermodynamic (naphthyridinone) product. Under FVP conditions, 6-substituted pyridopyrimidinones were obtained in high regioselectivity, which was not demonstrated before under standard Gould–Jacobs reaction conditions. DFT calculations have been additionally performed to provide further insights into the mechanistic pathways of this specific Gould–Jacobs reaction.

Limitations of the Jacobs-Gould reaction using microwave irradiation

Smith, Robert B.,Faki, Hajira,Leslie, Ray

experimental part, p. 1492 - 1499 (2011/06/17)

Upon investigating the green synthesis of some antimicrobial quinolone compounds, some atypical ring-closing patterns were observed during the synthesis of various intermediates using the Jacobs-Gould reaction.

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