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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)-

Ethanaminium,N-[4-[[4-(diethylamino)phenyl][4-(ethylamino)-1-naphthalenyl]methylene]-2,5-cyclohexadien-1-ylidene]-N-ethyl-, chloride

CCNc1ccc(c2c1cccc2)C(=C1CCC(=[N+](CC)CC)CC1)c1ccc(cc1)N(CC)CC.[Cl-] Request for Quotation
Chemical Name: Ethanaminium,N-[4-[[4-(diethylamino)phenyl][4-(ethylamino)-1-naphthalenyl]methylene]-2,5-cyclohexadien-1-ylidene]-N-ethyl-, chloride
CAS Number: 2390-60-5
Product Number: AG003VAT(AGN-PC-0QZXWU)
Synonyms:
MDL No:
Molecular Formula: C33H44ClN3
Molecular Weight: 518.1756

Identification/Properties

Properties
BP:
612.2°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
514.154g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
9
Exact Mass:
513.291g/mol
Monoisotopic Mass:
513.291g/mol
Topological Polar Surface Area:
20.4A^2
Heavy Atom Count:
37
Formal Charge:
0
Complexity:
722
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

GHS Pictogram:
Signal Word:
Danger
UN#:
3143
Hazard Statements:
H301-H319-H400
Precautionary Statements:
P273-P301+P310-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound N-(4-((4-(Diethylamino)phenyl)(4-(ethylamino)naphthalen-1-yl)methylene)cyclohexa-2,5-dien-1-ylidene)-N-ethylethanaminium chloride finds significant application in chemical synthesis as a versatile reagent. Its unique structural features make it an important building block for the synthesis of various organic molecules with complex structures. Due to its electron-rich nature and conjugated system, this compound can participate in a range of reactions such as nucleophilic addition, substitution, and electrophilic aromatic substitution. Its ability to act as both a nucleophile and an electrophile makes it highly valuable in the creation of asymmetric compounds and chiral molecules. Furthermore, the presence of multiple functional groups in this compound allows for the introduction of diverse chemical moieties in target molecules, facilitating the synthesis of new materials or pharmaceutical compounds with tailored properties. Additionally, the presence of the quaternary ammonium chloride salt group enhances the compound's solubility in various solvents, making it a versatile reagent in different reaction conditions.