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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)-

Piperidine, 1,1'-carbonothioylbis-

S=C(N1CCCCC1)N1CCCCC1 Request for Quotation
Chemical Name: Piperidine, 1,1'-carbonothioylbis-
CAS Number: 1013-92-9
Product Number: AG00046M(AGN-PC-0NJA42)
Synonyms:
MDL No:
Molecular Formula: C11H20N2S
Molecular Weight: 212.3549

Identification/Properties

Properties
BP:
140-160°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
212.355g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
212.135g/mol
Monoisotopic Mass:
212.135g/mol
Topological Polar Surface Area:
38.6A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
174
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335-H412
Precautionary Statements:
P261-P273-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


$Name$ is a versatile compound that finds widespread application in chemical synthesis, particularly in the field of organometallic chemistry. As a bidentate ligand, it is known for its ability to form stable coordination complexes with a variety of metal ions, such as copper, nickel, and platinum. These complexes have been utilized in a range of catalytic reactions, including cross-coupling reactions, hydrogenation reactions, and C-H activation. Dipentamethylene thiourea plays a crucial role in facilitating these reactions by stabilizing the metal center and influencing the reactivity of the coordinated metal species. Its unique coordination properties make it a valuable tool for the development of new methodologies in organic synthesis and materials chemistry.