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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)-

1-[5-(dimethylamino)naphthalen-1-yl]sulfonyl-3-ethylthiourea

CCNC(=S)NS(=O)(=O)c1cccc2c1cccc2N(C)C Request for Quotation
Chemical Name: 1-[5-(dimethylamino)naphthalen-1-yl]sulfonyl-3-ethylthiourea
CAS Number: 186661-19-8
Product Number: AG00AKFQ(AGN-PC-0KSFY7)
Synonyms:
MDL No:
Molecular Formula: C15H19N3O2S2
Molecular Weight: 337.4603

Identification/Properties

Computed Properties
Molecular Weight:
337.456g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
337.092g/mol
Monoisotopic Mass:
337.092g/mol
Topological Polar Surface Area:
102A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
488
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-Dansyl-N'-ethylthiourea is a versatile compound commonly used in chemical synthesis as a reagent for the derivatization and analysis of various amine-containing compounds. This unique compound contains a dansyl fluorescein moiety which provides it with fluorescent properties, making it especially useful in fluorescence-based assays and detection methods. In chemical synthesis, N-Dansyl-N'-ethylthiourea can be utilized as a derivatizing agent for the analysis of primary and secondary amines, allowing for their selective detection and quantification in complex mixtures. Additionally, this compound has been employed in the synthesis of novel fluorescent probes and sensors for biological applications, demonstrating its significance in the field of chemical biology and bioanalytical chemistry.