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5-Bromo-2-Chloro-N-[2-(Ethylamino)-3-Pyridinyl]-3-Pyridinecarboxamide is a complex chemical compound characterized by its unique molecular structure. It features a 5-bromo-2-chloro group, ethylamino and pyridinyl functional groups, and a pyridinecarboxamide moiety. 5-Bromo-2-Chloro-N-[2-(Ethylamino)-3-Pyridinyl]-3-Pyridinecarboxamide holds potential in various fields, including pharmaceuticals, agrochemicals, and materials science, due to its distinctive structural and property attributes. Its capacity for biological and chemical activities positions it as a promising candidate for further research and development.

380378-90-5

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  • 3-Pyridinecarboxamide,5-bromo-2-chloro-N-[2-(ethylamino)-3-pyridinyl]-

    Cas No: 380378-90-5

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380378-90-5 Usage

Uses

Used in Pharmaceutical Industry:
5-Bromo-2-Chloro-N-[2-(Ethylamino)-3-Pyridinyl]-3-Pyridinecarboxamide is used as a precursor in the synthesis of new drugs for its potential medicinal properties. Its unique structure allows for the development of compounds that could target specific biological pathways or receptors, offering novel therapeutic options for various diseases.
Used in Agrochemical Industry:
In the agrochemical sector, 5-Bromo-2-Chloro-N-[2-(Ethylamino)-3-Pyridinyl]-3-Pyridinecarboxamide is utilized as a building block for the creation of new pesticides. Its chemical composition can be tailored to target specific pests or diseases, enhancing crop protection and potentially reducing the environmental impact of traditional pesticides.
Used in Materials Science:
5-Bromo-2-Chloro-N-[2-(Ethylamino)-3-Pyridinyl]-3-Pyridinecarboxamide is employed in the development of advanced materials for its potential to influence material properties. Its incorporation into polymers or other materials could lead to new applications in areas such as electronics, coatings, or sensors, where specific chemical or physical characteristics are required.
Used in Research and Development:
5-Bromo-2-Chloro-N-[2-(Ethylamino)-3-Pyridinyl]-3-Pyridinecarboxamide serves as a subject of interest in research and development for its potential biological and chemical activities. Scientists explore its interactions with biological systems and its reactivity in chemical processes to uncover new applications and understand its full potential in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 380378-90-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,0,3,7 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 380378-90:
(8*3)+(7*8)+(6*0)+(5*3)+(4*7)+(3*8)+(2*9)+(1*0)=165
165 % 10 = 5
So 380378-90-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H12BrClN4O/c14-8-6-9(12(15)18-7-8)13(20)19-11-2-1-5-17-10(11)3-4-16/h1-2,5-7H,3-4,16H2,(H,19,20)

380378-90-5Relevant articles and documents

NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS

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Page 21, (2010/02/06)

Compounds represented by formula (1), wherein R1 is H, halogen, (C1-4)alkyl, O(C1-4)alkyl, and haloalkyl; R2 is H or methyl; R3 is H or (C1-4)alkyl; R4 is H or (C1-4)a

Non-nucleoside reverse transcriptase inhibitors

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Page 8, (2010/02/07)

Compounds represented by formula I: wherein R1 is H, halogen, (C1-4)alkyl, O(C1-4)alkyl, and haloalkyl; R2 is H or (C1-4)alkyl; R3 is H or (C1-4)alkyl; R4 is (C1-4)alkyl, (C1-4)alkyl(C3-7)cycloalkyl, or (C3-7)cycloalkyl; and Q is a fused phenyl-5 or 6-membered saturated heterocycle having one to two heteroatoms selected from O and N, said Q being optionally substituted with hydroxy, or (C1-4)alkyl which in turn maybe optionally substituted with pyridinyl-N-oxide or C(O)OR wherein R is H or (C1-4)alkyl; or a salt thereof. The compounds have inhibitory activity against Wild Type, and single and double mutants strains, of HIV.

Non-nucleoside reverse transcriptase inhibitors

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, (2008/06/13)

Provided are compounds of the general formula I: wherein R2 is selected from the group consisting of H, F, Cl, (C1-4) alkyl, (C3-4) cycloalkyl and CF3; R4 is H or Me; R5 is H, Me or Et, wit

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