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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, (4-methoxyphenyl)-

COc1ccc(cc1)NC(=S)N Request for Quotation
Chemical Name: Thiourea, (4-methoxyphenyl)-
CAS Number: 2293-07-4
Product Number: AG002LJM(AGN-PC-0JUNU6)
Synonyms:
MDL No:
Molecular Formula: C8H10N2OS
Molecular Weight: 182.2428

Identification/Properties

Properties
MP:
223-225 °C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
182.241g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
182.051g/mol
Monoisotopic Mass:
182.051g/mol
Topological Polar Surface Area:
79.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
155
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:
Danger
UN#:
2811
Hazard Statements:
H301
Precautionary Statements:
P301+P310
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(4-Methoxyphenyl)thiourea, also known as MPPT, is a versatile chemical reagent widely utilized in chemical synthesis processes. Due to its unique properties, this compound serves as a crucial building block in the creation of various pharmaceuticals, agricultural chemicals, and materials. In chemical synthesis, 1-(4-Methoxyphenyl)thiourea plays a significant role as a key intermediate in the production of diverse organic compounds. Its ability to undergo selective reactions makes it a valuable tool for introducing specific functional groups into target molecules. Additionally, the presence of a thiourea functional group enhances its utility in catalytic applications, promoting efficient and controlled transformations in complex chemical reactions. Overall, the application of 1-(4-Methoxyphenyl)thiourea in chemical synthesis enables the development of innovative compounds with tailored properties and applications.