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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, ethyl-

CCNC(=S)N Request for Quotation
Chemical Name: Thiourea, ethyl-
CAS Number: 625-53-6
Product Number: AG003QJN(AGN-PC-0AM6K1)
Synonyms:
MDL No:
Molecular Formula: C3H8N2S
Molecular Weight: 104.1740

Identification/Properties

Properties
MP:
108-110 °C(lit.)
BP:
132 °C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.5500 (estimate)
Solubility:
methanol: soluble25mg/mL, clear, colorless
Computed Properties
Molecular Weight:
104.171g/mol
XLogP3:
-0.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
104.041g/mol
Monoisotopic Mass:
104.041g/mol
Topological Polar Surface Area:
70.1A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
52.8
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:
P264-P270-P301+P310+P330-P405-P501
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-Ethylthiourea is a versatile chemical compound that finds valuable applications in various chemical synthesis processes. This compound is commonly utilized as a catalyst or reagent in organic reactions due to its unique properties and reactivity. In chemical synthesis, N-Ethylthiourea acts as a powerful nucleophile, enabling it to participate in nucleophilic substitution reactions. It can also function as a chelating agent, forming stable complexes with metal ions that facilitate specific chemical transformations. Its ability to selectively bind to certain metal ions makes it a valuable tool in coordination chemistry and metal-mediated organic reactions. Additionally, N-Ethylthiourea has been employed in the preparation of pharmaceutical intermediates, agrochemicals, and functional materials, showcasing its significance in modern synthetic chemistry.