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  2. Benzeneacetic acid, 2-[(2,6-dichlorophenyl)amino]-, compd. with1-pyrrolidineethanol (1:1)OTHER CA INDEX NAMES:1-Pyrrolidineethanol, 2-[(2,6-dichlorophenyl)amino]benzeneacetate(salt)

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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)-

Benzeneacetic acid, 2-[(2,6-dichlorophenyl)amino]-, compd. with1-pyrrolidineethanol (1:1)OTHER CA INDEX NAMES:1-Pyrrolidineethanol, 2-[(2,6-dichlorophenyl)amino]benzeneacetate(salt)

OC(=O)Cc1ccccc1Nc1c(Cl)cccc1Cl.OCCN1CCCC1 Request for Quotation
Chemical Name: Benzeneacetic acid, 2-[(2,6-dichlorophenyl)amino]-, compd. with1-pyrrolidineethanol (1:1)OTHER CA INDEX NAMES:1-Pyrrolidineethanol, 2-[(2,6-dichlorophenyl)amino]benzeneacetate(salt)
CAS Number: 119623-66-4
Product Number: AG000PDN(AGN-PC-0PDJW8)
Synonyms:
MDL No:
Molecular Formula: C20H24Cl2N2O3
Molecular Weight: 411.3222

Identification/Properties

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


The compound 2-(Pyrrolidin-1-yl)ethan-1-ol 2-(2-((2,6-dichlorophenyl)amino)phenyl)acetate is a versatile chemical intermediate commonly employed in chemical synthesis processes. It is utilized as a key building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique reactivity and structural properties. In chemical synthesis, this compound serves as an important precursor in the formation of complex organic molecules, allowing chemists to introduce specific functional groups and structural motifs into target compounds. Its pyrrolidine and phenyl acetate moieties enable diverse derivatization reactions, facilitating the synthesis of novel compounds with desired properties.Additionally, the presence of the 2,6-dichlorophenylamino group provides an avenue for further modifications through selective substitution or coupling reactions. This enables the customization of the final products for specific applications in medicinal chemistry, material science, and other fields that require tailored chemical structures.Overall, the strategic incorporation of 2-(Pyrrolidin-1-yl)ethan-1-ol 2-(2-((2,6-dichlorophenyl)amino)phenyl)acetate in chemical synthesis processes allows for the efficient and precise construction of diverse organic compounds with potential pharmaceutical, agricultural, or industrial applications.