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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)-

Ethanone, 1-[6-(dimethylamino)-2-naphthalenyl]-

CN(c1ccc2c(c1)ccc(c2)C(=O)C)C Request for Quotation
Chemical Name: Ethanone, 1-[6-(dimethylamino)-2-naphthalenyl]-
CAS Number: 68520-00-3
Product Number: AG006345(AGN-PC-00OWTK)
Synonyms:
MDL No:
Molecular Formula: C14H15NO
Molecular Weight: 213.2750

Identification/Properties

Properties
MP:
149-153°C
BP:
373.832°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
213.28g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
213.115g/mol
Monoisotopic Mass:
213.115g/mol
Topological Polar Surface Area:
20.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
262
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-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


$Name$ is a versatile compound commonly used in chemical synthesis due to its unique properties and reactivity. Specifically, 1-(6-(Dimethylamino)naphthalen-2-yl)ethanone plays a crucial role as a key intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its functional groups enable it to participate in important reactions such as nucleophilic addition, acylation, and reduction, making it an essential building block in organic synthesis. Additionally, this compound serves as a valuable fluorescent probe in biochemical research, aiding in the study of protein interactions and cellular processes.