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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)-

thiophene-2-carboximidamide;hydrochloride

NC(=N)c1cccs1.Cl Request for Quotation
Chemical Name: thiophene-2-carboximidamide;hydrochloride
CAS Number: 54610-70-7
Product Number: AG00D8X2(AGN-PC-0KL16Q)
Synonyms:
MDL No:
Molecular Formula: C5H7ClN2S
Molecular Weight: 162.6405

Identification/Properties

Computed Properties
Molecular Weight:
162.635g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
162.002g/mol
Monoisotopic Mass:
162.002g/mol
Topological Polar Surface Area:
78.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
103
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amidinothiophene hydrochloride, a versatile chemical compound, plays a pivotal role in chemical synthesis. As a key reagent, it serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and organic compounds. Its unique structural properties make it an essential component in the development of drugs, particularly those targeting neurological disorders, cardiovascular diseases, and infectious illnesses. Moreover, its application extends to the synthesis of complex heterocyclic compounds, showcasing its significance in medicinal chemistry and material science. The incorporation of 2-Amidinothiophene hydrochloride in chemical reactions enables the formation of diverse molecular structures, thereby facilitating advancements in drug discovery, material engineering, and scientific research.