Acetamide, 2-(phenylamino)-|21969-70-0,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

Acetamide, 2-(phenylamino)-

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Chemical Name:	Acetamide, 2-(phenylamino)-
CAS Number:	21969-70-0
Product Number:	AG00C2QO(AGN-PC-00P0YH)
Synonyms:
MDL No:	MFCD08691108
Molecular Formula:	C8H10N2O
Molecular Weight:	150.1778

Identification/Properties
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Identification/Properties

Computed Properties

Molecular Weight:

150.181g/mol

XLogP3:

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

150.079g/mol

Monoisotopic Mass:

150.079g/mol

Topological Polar Surface Area:

55.1A^2

Heavy Atom Count:

Formal Charge:

Complexity:

130

Isotope Atom Count:

Defined Atom Stereocenter Count:

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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

2-Anilinoacetamide is a versatile compound commonly used in chemical synthesis for its unique properties and applications. In the field of organic chemistry, this compound serves as a key intermediate in the synthesis of various important organic molecules and pharmaceuticals. Its structure contains both an aniline group and an acetamide group, making it a valuable building block for creating complex organic structures through various chemical reactions.In chemical synthesis, 2-Anilinoacetamide acts as a precursor for the preparation of diverse compounds, especially those with biological activity. It can undergo various transformations such as acylation, alkylation, and condensation reactions to yield structurally diverse products. One of its significant applications is in the synthesis of heterocyclic compounds, which are essential in medicinal chemistry for developing new pharmaceutical agents.Moreover, 2-Anilinoacetamide plays a crucial role in the production of dyes, pigments, and agricultural chemicals. Its reactivity and versatility make it an indispensable component in the manufacturing process of these products. Additionally, it is utilized as a reagent in the preparation of polymer materials and as a starting material for the synthesis of various specialty chemicals.Overall, the application of 2-Anilinoacetamide in chemical synthesis spans across a wide range of industries, from pharmaceuticals to materials science, highlighting its importance as a key compound for creating valuable and diverse chemical products.