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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)-

Thiourea, (2,6-diethylphenyl)-

CCc1cccc(c1NC(=S)N)CC Request for Quotation
Chemical Name: Thiourea, (2,6-diethylphenyl)-
CAS Number: 25343-30-0
Product Number: AG00C1WB(AGN-PC-0JV8UZ)
Synonyms:
MDL No:
Molecular Formula: C11H16N2S
Molecular Weight: 208.3231

Identification/Properties

Properties
MP:
196-198℃
Form:
Solid
Computed Properties
Molecular Weight:
208.323g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
208.103g/mol
Monoisotopic Mass:
208.103g/mol
Topological Polar Surface Area:
70.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
182
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#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(2,6-Diethylphenyl)thiourea is a versatile compound that finds widespread application in organic chemical synthesis. It serves as a valuable building block in the preparation of various organic compounds due to its unique reactivity and structural properties. In chemical synthesis, this compound is commonly used as a precursor for the synthesis of heterocyclic compounds, pharmaceutical intermediates, and agrochemicals. Its thiourea functionality enables it to participate in a variety of reactions, including cyclization, alkylation, and substitution reactions, leading to the formation of diverse molecular structures. Additionally, 1-(2,6-Diethylphenyl)thiourea has proven to be an efficient ligand in transition metal-catalyzed reactions, enhancing the selectivity and efficiency of various transformations. Its applications extend to the field of materials science, where it is employed in the preparation of advanced materials with tailor-made properties. Overall, the versatility and reactivity of 1-(2,6-Diethylphenyl)thiourea make it a valuable tool in the realm of chemical synthesis, enabling the creation of complex organic molecules with diverse functionalities.