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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)-

2-Thiophenecarboximidamide

NC(=N)c1cccs1 Request for Quotation
Chemical Name: 2-Thiophenecarboximidamide
CAS Number: 54610-75-2
Product Number: AG00DEHH(AGN-PC-0KL16R)
Synonyms:
MDL No:
Molecular Formula: C5H6N2S
Molecular Weight: 126.17954

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Thiophene-2-carboximidamide is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. In organic chemistry, it serves as a key building block for the construction of various heterocyclic compounds. The presence of the thiophene ring imparts favorable electronic characteristics, making it a valuable precursor in the development of pharmaceuticals, agrochemicals, and materials science. Its ability to undergo functional group transformations enables the introduction of diverse functionalities, enhancing the structural diversity and complexity of synthesized molecules. Additionally, Thiophene-2-carboximidamide plays a crucial role in the creation of novel organic frameworks with potential applications in medicinal chemistry and materials design. Through strategic manipulation of its chemical reactivity, researchers can access a wide array of molecular scaffolds, driving innovation in synthetic methodologies and facilitating the discovery of new chemical entities.