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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)-

3-Thiophenecarbonitrile, 2-amino-4-hydroxy-

N#Cc1c(N)scc1O Request for Quotation
Chemical Name: 3-Thiophenecarbonitrile, 2-amino-4-hydroxy-
CAS Number: 99580-50-4
Product Number: AG00IKB7(AGN-PC-00N0EG)
Synonyms:
MDL No:
Molecular Formula: C5H4N2OS
Molecular Weight: 140.1631

Identification/Properties

Computed Properties
Molecular Weight:
140.16g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
140.004g/mol
Monoisotopic Mass:
140.004g/mol
Topological Polar Surface Area:
98.3A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
152
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:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amino-4-hydroxythiophene-3-carbonitrile, also known as $name$, is a versatile chemical compound that finds wide application in chemical synthesis. Its unique structure and properties make it a valuable building block in the creation of various organic compounds.In chemical synthesis, $name$ serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Its presence in reactions facilitates the formation of new bonds and functional groups, allowing for the creation of complex molecular structures in a controlled manner.One of the prominent applications of 2-Amino-4-hydroxythiophene-3-carbonitrile is in the synthesis of heterocyclic compounds, which are essential components in the development of drugs and materials with specific properties. By incorporating $name$ into reactions, chemists can access a diverse range of derivatives with varying biological activities and physical characteristics.Moreover, the presence of the amino and hydroxy functional groups in 2-Amino-4-hydroxythiophene-3-carbonitrile enables further derivatization, leading to the synthesis of compounds with enhanced solubility, stability, or reactivity. This flexibility makes it a valuable tool for researchers and synthetic chemists seeking to design novel molecules for specific applications.