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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, (aminoiminomethyl)-

NN=CNC(=S)N Request for Quotation
Chemical Name: Thiourea, (aminoiminomethyl)-
CAS Number: 2114-02-5
Product Number: AG002LC5(AGN-PC-0O7TLN)
Synonyms:
MDL No:
Molecular Formula: C2H6N4S
Molecular Weight: 118.1608

Identification/Properties

Properties
MP:
171-173 °C(lit.)
BP:
310.5°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.5605 (estimate)
Computed Properties
Molecular Weight:
118.158g/mol
XLogP3:
-1.3
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
118.031g/mol
Monoisotopic Mass:
118.031g/mol
Topological Polar Surface Area:
123A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
102
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
Precautionary Statements:
P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Guanylthiourea is a versatile chemical compound that finds wide application in chemical synthesis processes. As a powerful nucleophilic reagent, Guanylthiourea serves as a valuable building block in the creation of various organic compounds. One of its key applications lies in the field of medicinal chemistry, where it is utilized in the synthesis of pharmaceutical agents and drugs. Additionally, Guanylthiourea plays a crucial role in the development of complex organic molecules and functional materials through its involvement in multi-step synthesis pathways. This compound's unique reactivity and structural characteristics make it a valuable tool for chemists seeking to design and construct novel compounds with specific properties and functionalities.