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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)-

Guanidine, ethyl-, monohydrochloride

CCNC(=N)N.Cl Request for Quotation
Chemical Name: Guanidine, ethyl-, monohydrochloride
CAS Number: 19341-54-9
Product Number: AG003T0D(AGN-PC-0QM41E)
Synonyms:
MDL No:
Molecular Formula: C3H10ClN3
Molecular Weight: 123.5846

Identification/Properties

Properties
MP:
115-118℃
Storage:
Room Temperature;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
123.584g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
123.056g/mol
Monoisotopic Mass:
123.056g/mol
Topological Polar Surface Area:
64.4A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
53.1
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Ethylguanidine hydrochloride is a versatile chemical compound that finds application in various chemical synthesis processes. It serves as a key reagent in the formation of a variety of organic compounds due to its unique properties and reactivity. In chemical synthesis, 1-Ethylguanidine hydrochloride is often used as a catalyst or as a precursor in the production of pharmaceutical intermediates, agrochemicals, and specialty chemicals. Its ability to participate in diverse reaction mechanisms makes it a valuable tool for the efficient and selective creation of complex molecular structures. Additionally, 1-Ethylguanidine hydrochloride has been employed in the synthesis of heterocyclic compounds and has shown promising results in the development of novel chemical entities with potential applications in drug discovery and material science. Its role in facilitating key bond formations and functional group transformations highlights its significance in modern organic synthesis strategies.