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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)-

Carbamic acid, [[(2-aminophenyl)amino]thioxomethyl]-, methyl ester

COC(=O)NC(=S)Nc1ccccc1N Request for Quotation
Chemical Name: Carbamic acid, [[(2-aminophenyl)amino]thioxomethyl]-, methyl ester
CAS Number: 27079-29-4
Product Number: AG003S13(AGN-PC-0KO6AP)
Synonyms:
MDL No:
Molecular Formula: C9H11N3O2S
Molecular Weight: 225.2675

Identification/Properties

Properties
MP:
184-185°C
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
225.266g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
225.057g/mol
Monoisotopic Mass:
225.057g/mol
Topological Polar Surface Area:
109A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
248
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


Methyl [(2-aminophenyl)carbamothioyl]carbamate, also known by its chemical formula C9H10N2O2S, is a versatile compound widely used in chemical synthesis applications. This compound plays a crucial role in various organic reactions and has become a valuable tool for chemists in the laboratory.One of the main applications of Methyl [(2-aminophenyl)carbamothioyl]carbamate is as a reagent in the synthesis of heterocyclic compounds. It is particularly useful in the formation of thiazolidine derivatives, which have diverse pharmacological properties and are found in many biologically active molecules. The presence of both an amine and a thiol functional group in this compound makes it a valuable building block for creating complex organic structures.Furthermore, Methyl [(2-aminophenyl)carbamothioyl]carbamate can participate in various coupling reactions to form new carbon-carbon or carbon-nitrogen bonds. Its unique structure provides opportunities for chemists to design novel molecules with specific properties and functionalities.Overall, this compound's role in chemical synthesis extends beyond its basic structure, offering a wide range of possibilities for creating innovative compounds in both academic research and industrial settings.