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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)-

1H-Imidazole, 2-[(1-methylpropyl)dithio]-

CCC(SSc1ncc[nH]1)C Request for Quotation
Chemical Name: 1H-Imidazole, 2-[(1-methylpropyl)dithio]-
CAS Number: 141400-58-0
Product Number: AG007ZET(AGN-PC-0JN9CJ)
Synonyms:
MDL No: MFCD18086851
Molecular Formula: C7H12N2S2
Molecular Weight: 188.3136

Identification/Properties

Computed Properties
Molecular Weight:
188.307g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
188.044g/mol
Monoisotopic Mass:
188.044g/mol
Topological Polar Surface Area:
79.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
111
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


PX-12, also known as auranofin, is a potent organic compound that finds versatile application in the realm of chemical synthesis. With its unique structure and reactivity, PX-12 exhibits remarkable potential in various synthetic processes, particularly in the realm of organic chemistry.In chemical synthesis, PX-12 serves as a valuable tool for the creation of complex molecules through diverse reactions such as oxidation, reduction, and coordination. Its ability to participate in redox reactions makes it a key player in the development of novel compounds with desired properties. Through its interaction with various functional groups, PX-12 can facilitate the formation of crucial chemical bonds, ultimately leading to the synthesis of intricate molecular structures.Furthermore, PX-12's compatibility with different solvents and reaction conditions enhances its utility in a wide range of synthetic applications. Whether employed as a catalyst, reagent, or precursor, PX-12 displays consistent performance, making it a reliable choice for chemists seeking to achieve precise and efficient synthesis of target molecules.Overall, PX-12 stands as a versatile and indispensable component in the toolkit of synthetic chemists, offering a robust platform for the exploration and development of innovative chemical processes.