1020252-22-5 Usage
Benzene ring
Attached to a nitrile group
The benzene ring is a six-carbon ring with alternating single and double bonds, and it is connected to a nitrile group (C≡N), which is a carbon-nitrogen triple bond.
3. 2,2-Dimethyl-4,6-dioxo-[1,3]dioxan-5-ylideneMethyl unit
This unit is a structural part of the compound, consisting of a five-membered dioxane ring with two methyl groups at the 2-position, two oxygen atoms at the 4and 6-positions, and a methylidene group (CH2) at the 5-position.
Aminomethyl group
Connected to the benzene ring
The aminomethyl group (NH2-CH2) is attached to the benzene ring, which may contribute to the compound's reactivity and potential applications.
Nitrile group
Attached to the benzene ring
The nitrile group (C≡N) is connected to the benzene ring and is responsible for the compound's cyano (-CN) functional group.
Potential applications
Pharmaceuticals, organic synthesis, or as a component in the production of other chemicals
The presence of the aminomethyl and nitrile groups suggests that this compound may have potential applications in various fields, such as pharmaceuticals, organic synthesis, or as a building block for other chemical compounds.
Specific properties and potential uses
Depend on further research and testing
The exact properties and potential uses of this compound would need to be determined through additional research, experimentation, and testing to fully understand its capabilities and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1020252-22-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,0,2,5 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1020252-22:
(9*1)+(8*0)+(7*2)+(6*0)+(5*2)+(4*5)+(3*2)+(2*2)+(1*2)=65
65 % 10 = 5
So 1020252-22-5 is a valid CAS Registry Number.
1020252-22-5Relevant articles and documents
Regioselective synthesis of quinolin-4-ones by pyrolysis of anilinomethylene derivatives of Meldrum's acid
Hill, Lawrence,Imam, S. Haider,McNab, Hamish,O'Neill, William J.
experimental part, p. 1847 - 1851 (2009/12/05)
Electron-rich and electron-deficient anilinomethylene derivatives of Meldrum's acid cyclize equally efficiently to quinolin-4-ones via imidoylketene intermediates under flash vacuum pyrolysis (FVP) conditions. Georg Thieme Verlag Stuttgart.
INDAZOLE/PYRZOLO[4,3-c]PYRIDIN DERIVATIVES AS JNK INHIBITORS, COMPOSITIONS AND METHODS RELATED THERETO AS WELL AS INTERMEDIATE THEREOF
-
Page 29, (2008/06/13)
The present invention relates to new compounds of formula (I) in which:X is CR4 or N; R1 is -OR5, -NHCOR6 or -NR6R7; R2 is hydrogen, Oar1 or -NHAr1 wherein Ar1 is aryl optionally substituted with one or more of R8, -OR8, -NR8R9, -CONR8R9, -COOR8, -NR8COR9, -SR8, -SO2NR8R9, -NR8SO2 R9, halogen, cyano, or nitro; R3 is hydrogen or -NHAr2 wherein Ar2 is benzene optionally substituted with one or more of R8, -OR8, -NR8R9, halogen or nitro, wherein R2 and R3 is not simultaneously hydrogen; a process for their preparation and new intermediates used therein, pharmaceutical formulations containing said therapeutically active compounds and to the use of said active compounds in therapy.
