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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

N-(4-Chlorobenzyl)-1-(5-nitrothiophen-2-yl)methanamine

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Chemical Name: N-(4-Chlorobenzyl)-1-(5-nitrothiophen-2-yl)methanamine
CAS Number: 1384516-10-2
Product Number: AG01E1RK(AGN-PC-0WAG3X)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


N-(4-Chlorobenzyl)-1-(5-nitrothiophen-2-yl)methanamine is a versatile compound commonly employed in chemical synthesis as a key intermediate. Its unique structure serves as a building block for the creation of various organic molecules with diverse functionalities. This compound plays a crucial role in the formation of advanced materials, pharmaceuticals, and agrochemicals through its ability to undergo selective transformations and participate in complex reactions. The application of N-(4-Chlorobenzyl)-1-(5-nitrothiophen-2-yl)methanamine in chemical synthesis showcases its significance in the development of novel compounds with potential industrial and scientific utility.