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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)-

Phenol, 2-(ethylamino)-

CCNc1ccccc1O Request for Quotation
Chemical Name: Phenol, 2-(ethylamino)-
CAS Number: 614-70-0
Product Number: AG0036ZN(AGN-PC-0JL8V7)
Synonyms:
MDL No:
Molecular Formula: C8H11NO
Molecular Weight: 137.1790

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
137.182g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
137.084g/mol
Monoisotopic Mass:
137.084g/mol
Topological Polar Surface Area:
32.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
95.3
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Phenol, 2-(ethylamino)-, also known as ethylamino phenol, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This compound is commonly utilized as a key building block in the production of various organic compounds, serving as a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, Phenol, 2-(ethylamino)- plays a crucial role as a nucleophilic reagent, participating in a range of reactions such as nucleophilic substitution, acylation, and condensation reactions. Its ethylamino group can act as a strong nucleophile, allowing for the formation of new carbon-carbon or carbon-heteroatom bonds in the presence of suitable electrophiles.Additionally, Phenol, 2-(ethylamino)- can undergo various functional group transformations, enabling the introduction of different chemical functionalities into the molecule. This versatility makes it a valuable tool for designing and synthesizing complex organic molecules with specific properties and functions.Overall, the application of Phenol, 2-(ethylamino)- in chemical synthesis provides chemists with a powerful tool for the efficient construction of diverse organic compounds with potential applications in drug discovery, material science, and various other fields.