1002-19-3 Usage
General Description
3-[(3-Amino-3-oxopropyl)dithio]propanamide is a chemical compound with the molecular formula C6H12N2O2S2. It is a thiol derivative and contains both amine and oxopropyl functional groups. 3-[(3-AMINO-3-OXOPROPYL)DITHIO]PROPANAMIDE has potential applications in medicinal chemistry and drug development due to its unique structural features. It may also have potential uses as a building block in organic synthesis and materials science. Further research and investigation are needed to fully understand the properties and potential uses of 3-[(3-Amino-3-oxopropyl)dithio]propanamide.
Check Digit Verification of cas no
The CAS Registry Mumber 1002-19-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1002-19:
(6*1)+(5*0)+(4*0)+(3*2)+(2*1)+(1*9)=23
23 % 10 = 3
So 1002-19-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H12N2O2S2/c1-3(5(7)9)11-12-4(2)6(8)10/h3-4H,1-2H3,(H2,7,9)(H2,8,10)/p-2
1002-19-3Relevant articles and documents
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Knunyants,I.L. et al.
, (1965)
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TETRAHYDROPYRAZOLO-PYRAZINYL-DIHYDROIMIDAZOLONE OR TETRAHYDROPYRAZOLO-PYRIDINYL-DIHYDROIMIDAZOLONE COMPOUNDS AND METHODS OF USING SAME
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Paragraph 00562, (2022/02/05)
The application relates to a compound of Formula (I) : or a pharmaceutically acceptable salt, hydrate, solvate, prodrug, stereoisomer, or tautomer thereof, which modulates the activity of GLP-1 receptor, a pharmaceutical composition comprising a compound of Formula (I), and a method of treating or preventing a disease in which GLP-1 receptor plays a role.
Synthesis and antibacterial activity of 2-(4-substituted phenyl)-3(2H)-isothiazolones
Khalaj, Ali,Adibpour, Neda,Shahverdi, Ahmad Reza,Daneshtalab, Mohsen
, p. 699 - 705 (2007/10/03)
Several new and known 2-(4-substituted phenyl)-3(2H)-isothiazolone derivatives with or without chloro substituent at C-5 position were synthesized and their in vitro antibacterial activity against selected Gram-negative and Gram-positive bacteria were eva
