1221153-82-7 Usage
Description
4-(5-Chloro-1-isopropyl-1H-pyrrolo[2,3-c]pyridin-3-yl)pyrimidin-2-amine is a complex chemical compound characterized by its unique structure, which includes a pyrrolopyridine ring, a pyrimidine ring, an isopropyl group, and an amine group. It is identified by the molecular formula C13H14ClN5 and has a molecular weight of 279.74 g/mol. 4-(5-Chloro-1-isopropyl-1H-pyrrolo[2,3-c]pyridin-3-yl)pyrimidin-2-amine's synthesis and industrial applications are not extensively documented, indicating that it may be utilized in specialized research contexts. Due to its chemical properties, it is essential to handle this compound with appropriate safety precautions to mitigate potential reactivity and bioactivity.
Uses
Used in Academic Research:
4-(5-Chloro-1-isopropyl-1H-pyrrolo[2,3-c]pyridin-3-yl)pyrimidin-2-amine is used as a research compound for exploring its chemical properties and potential applications in various scientific fields. Its complex structure makes it a candidate for studies in organic chemistry, medicinal chemistry, and materials science.
Used in Industrial Research:
In industrial research, 4-(5-Chloro-1-isopropyl-1H-pyrrolo[2,3-c]pyridin-3-yl)pyrimidin-2-amine is used as a starting material or intermediate in the synthesis of more complex molecules, potentially for pharmaceuticals, agrochemicals, or other specialty chemicals. Its role in these applications is to provide a foundation for further chemical modifications and innovations.
Used in Drug Discovery:
4-(5-Chloro-1-isopropyl-1H-pyrrolo[2,3-c]pyridin-3-yl)pyrimidin-2-amine is used as a lead compound in drug discovery, where its structure may be optimized to develop new therapeutic agents. 4-(5-Chloro-1-isopropyl-1H-pyrrolo[2,3-c]pyridin-3-yl)pyrimidin-2-amine's potential bioactivity and reactivity make it a valuable candidate for screening in the search for new drugs.
Used in Chemical Synthesis:
In the field of chemical synthesis, 4-(5-Chloro-1-isopropyl-1H-pyrrolo[2,3-c]pyridin-3-yl)pyrimidin-2-amine is used as a building block for creating new chemical entities. Its presence in a molecule can contribute to the overall properties and reactivity of the final product, making it a versatile component in synthetic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1221153-82-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,1,1,5 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1221153-82:
(9*1)+(8*2)+(7*2)+(6*1)+(5*1)+(4*5)+(3*3)+(2*8)+(1*2)=97
97 % 10 = 7
So 1221153-82-7 is a valid CAS Registry Number.
1221153-82-7Relevant articles and documents
NOVEL 6-AZAINDOLE AMINOPYRIMIDINE DERIVATIVES HAVING NIK INHIBITORY ACTIVITY
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Page/Page column 42; 44; 45, (2010/04/28)
The present invention relates to a compound of formula I: wherein: R1 is C1-6 alkyl, C3-8 cycloalkyl, aryl, heterocyclyl, or -COR1x, where the C1-6 alkyl, C3-8 cycloalkyl, aryl, and heterocyclyl may be substituted; and R1x is C3-8 cycloalkyl, aryl, or heterocyclyl, any of which may be substituted; R2, R3, R4, R5, R6, and R7 are each independently hydrogen, halogen, C1-6 alkyl, or aryl, where the C1-6 alkyl or aryl may be substituted; R8 is hydrogen, C1-6 alkyl, aryl, or heterocyclyl, any of which may be substituted; or a pharmaceutically acceptable salt or ester thereof.
