77472-70-9

  • Product Name:4-Phenyl-2-pyrrolidone-1-acetamide
  • Molecular Formula:C12H14N2O2
  • Purity:99%
  • Molecular Weight:218.255
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Product Details;

CasNo: 77472-70-9

Molecular Formula: C12H14N2O2

Quality Manufacturer Supply 99% Pure 4-Phenyl-2-pyrrolidone-1-acetamide 77472-70-9 Cheapest Price

  • Molecular Formula:C12H14N2O2
  • Molecular Weight:218.255
  • Vapor Pressure:1.3E-09mmHg at 25°C 
  • Melting Point:129.5-130.5 °C(Solv: ethyl acetate (141-78-6)) 
  • Refractive Index:1.579 
  • Boiling Point:486.4 °C at 760 mmHg 
  • PKA:15.67±0.40(Predicted) 
  • Flash Point:247.9 °C 
  • PSA:64.39000 
  • Density:1.22 g/cm3 
  • LogP:1.57540 

4-Phenyl-2-pyrrolidone-1-acetamide(Cas 77472-70-9) Usage

Description

4-Phenyl-2-pyrrolidone-1-acetamide (also named as Phenylpiracetam, Fonturacetam) is a phenylated analog of the drug piracetam, which was developed in 1983 in Russia. It is now available as a prescription drug. It has antiamnesic, anticonvulsant and anxiolytic properties. It is used as a general stimulant or to increase tolerance to extreme temperatures and stress.

Uses

Carphedone is a GABA derivative that exhibited apparent immunocorrection properties during immunosuppression induced by cyclophosphamide were studied.

InChI:InChI=1/C12H14N2O2/c13-11(15)8-14-7-10(6-12(14)16)9-4-2-1-3-5-9/h1-5,10H,6-8H2,(H2,13,15)

77472-70-9 Relevant articles

Synthesis of substituted 2-(2-oxopyrrolidin-1-yl)acetamides

Kavina,Sizov,Yakovlev

, p. 873 - 878 (2017/08/02)

The reaction of chloroacetamide with 2 e...

Method for preparing phenyl piracetam

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Paragraph 0075; 0076; 0077; 0078; 0079; 0080-0088, (2017/05/09)

The invention discloses a method for pre...

SIMPLE METHODS FOR THE N-ALKYLATION OF LACTAMS

Kramarova, E. P.,Shipov, A. G.,Orlova, N. A.,Artamkina, O. B.,Belavin, I. Yu.,Baukov, Yu. I.

, p. 970 - 979 (2007/10/02)

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THE SYNTHESIS AND ANTISPASMODIC ACTIVITY OF 4-PHENYLPYRROLIDONE-2-ACETAMIDES

Glozman, O. M.,Morozov, I. S.,Zhmurenko, L. A.,Zagorevskii, V. A.

, p. 776 - 780 (2007/10/02)

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77472-70-9 Process route

methyl-2-oxo-4-phenylpyrrolidine-1-acetate
68497-63-2

methyl-2-oxo-4-phenylpyrrolidine-1-acetate

(RS)-2-(2-oxo-4-phenylpyrrolidin-1-yl)acetamide
77472-70-9

(RS)-2-(2-oxo-4-phenylpyrrolidin-1-yl)acetamide

Conditions
Conditions Yield
With ammonium hydroxide; for 2h;
81%
With ammonia; In methanol; at 20 - 30 ℃; for 12h; Concentration; Temperature; Solvent;
81%
2-oxo-4-phenyl-1-pyrrolidineacetic acid, ethyl ester
70291-40-6

2-oxo-4-phenyl-1-pyrrolidineacetic acid, ethyl ester

(RS)-2-(2-oxo-4-phenylpyrrolidin-1-yl)acetamide
77472-70-9

(RS)-2-(2-oxo-4-phenylpyrrolidin-1-yl)acetamide

Conditions
Conditions Yield
With ammonia; In methanol; at 45 - 50 ℃; for 5h;
100%
With ammonium hydroxide; for 2h;
64%

77472-70-9 Upstream products

  • 68497-63-2
    68497-63-2

    methyl-2-oxo-4-phenylpyrrolidine-1-acetate

  • 70291-40-6
    70291-40-6

    2-oxo-4-phenyl-1-pyrrolidineacetic acid, ethyl ester

  • 1198-97-6
    1198-97-6

    4-phenylpyrrolidin-2-one

  • 106869-48-1
    106869-48-1

    4-phenyl-1-(trimethylsilyl)-2-pyrrolidinone

77472-70-9 Downstream products

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    1613318-02-7

    C34H44N2O3

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