947017-65-4 Usage
Fused heterocyclic compound
Pyrrolopyridine ring system The compound consists of a fused ring structure containing both pyrrole and pyridine rings, which are heterocyclic (containing atoms other than carbon) in nature.
Thienyl substituent
At position 2 A thienyl group (a five-membered ring with one sulfur atom) is attached to the second position of the pyrrolopyridine ring system.
Applications in pharmaceutical industry
Building block for synthesis of biologically active compounds This chemical serves as an intermediate for creating various drug molecules, contributing to the development of new medications.
Applications in agrochemical industry
Pesticides The compound can be used as a precursor for the development of pesticides, which help protect crops from pests and diseases.
Interest in materials science
Organic electronic devices and optoelectronic materials Due to its unique electronic properties, the compound has potential applications in the development of organic electronic devices such as organic light-emitting diodes (OLEDs) and other optoelectronic materials.
Potential anticancer agent
Inhibiting cell proliferation Research has shown that this chemical may have anticancer properties by demonstrating the ability to inhibit the proliferation of cancer cells.
Check Digit Verification of cas no
The CAS Registry Mumber 947017-65-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,7,0,1 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 947017-65:
(8*9)+(7*4)+(6*7)+(5*0)+(4*1)+(3*7)+(2*6)+(1*5)=184
184 % 10 = 4
So 947017-65-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H8N2S/c1-3-8-7-9(10-4-2-6-14-10)13-11(8)12-5-1/h1-7H,(H,12,13)
947017-65-4Relevant academic research and scientific papers
Azaquinazoline Inhibitors Of Atypical Protein Kinase C
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Paragraph 0226; 0234, (2015/12/24)
The present application provides a compound of formula (I) and/or a salt thereof, wherein R1, G, and X are as defined herein. A compound of formula (I) and/or its salts have aPKC inhibitory activity, and may be used to treat proliferative disor
Synthesis of 2-substituted-7-azaindoles from 2-amino-3-picolin
Parcerisa, Javier,Romero, Manel,Pujol, Maria Dolors
, p. 500 - 507 (2008/03/27)
An easy route to the synthesis of 2-substituted-7-azaindole derivatives has been developed. The carbinol intermediate dissolved in DMF undergoes cyclization upon treatment with sodium hydride, trifluoroacetic anhydride, and trifluoroacetic acid at 120 °C
