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1-(2-hydroxy-2-phenylethyl)pyrrolidine-2,5-dione

  • CAS:68239-22-5
  • purity:99%
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Cosmetics Grade 1-(2-hydroxy-2-phenylethyl)pyrrolidine-2,5-dione 68239-22-5 For Sale with Good Price

  • Molecular Formula: C12H13NO3
  • Molecular Weight: 219.24
  • Vapor Pressure: 1.03E-08mmHg at 25°C 
  • Boiling Point: 445.4°Cat760mmHg 
  • Flash Point: 223.2°C 
  • PSA: 57.61000 
  • Density: 1.294g/cm3 
  • LogP: 0.80690 

1-(2-hydroxy-2-phenylethyl)pyrrolidine-2,5-dione(Cas 68239-22-5) Usage

Synonym

(S)-HPHPD

Classification

Pyrrolidine-2,5-dione derivative

Parent compound

Amino acid proline

Potential pharmaceutical application

Inhibitor of prolyl hydroxylase enzyme

Enzyme target

Prolyl hydroxylase

Enzyme function

Regulation of hypoxia-inducible factor (HIF)

HIF role

Oxygen homeostasis regulation

Associated diseases

Cancer, ischemic heart disease

Therapeutic potential

Treatment of conditions related to HIF pathway modulation

Current status

Further research needed to understand potential uses and mechanisms of action

General Description

1-(2-hydroxy-2-phenylethyl)pyrrolidine-2,5-dione, also known as (S)-HPHPD, is a chemical compound with a molecular formula C12H13NO3. It is a derivative of the amino acid proline and is classified as a pyrrolidine-2,5-dione. 1-(2-hydroxy-2-phenylethyl)pyrrolidine-2,5-dione has been studied for its potential as a pharmaceutical agent, particularly for its use as an inhibitor of the enzyme prolyl hydroxylase. Prolyl hydroxylase is involved in the regulation of hypoxia-inducible factor (HIF), which plays a role in oxygen homeostasis and is associated with diseases such as cancer and ischemic heart disease. (S)-HPHPD may have therapeutic applications in the treatment of these conditions by modulating the HIF pathway. Further research is needed to fully understand the potential uses and mechanisms of action of this compound.

InChI:InChI=1/C12H13NO3/c14-10(9-4-2-1-3-5-9)8-13-11(15)6-7-12(13)16/h1-5,10,14H,6-8H2

68239-22-5 Relevant articles

Preparation and Reactivity of Highly Functionalized Organometallics at the α Position of Oxygen or Nitrogen

Knochel, Paul,Chou, Tso-Sheng,Jubert, Carole,Rajagopal, Duddu

, p. 588 - 599 (2007/10/02)

α-Halogenoalkyl carboxylates (FG-R1CH(X)...

Base-catalyzed carbon-carbon bond formation reactions of ω-hydroxylactams

Speckamp, W. N.,Boer, J. J. J. de

, p. 410 - 414 (2007/10/02)

Active methylene compounds such as methy...

68239-22-5 Process route

succinic acid N-(chloromethyl)imide
54553-14-9

succinic acid N-(chloromethyl)imide

benzaldehyde
100-52-7

benzaldehyde

N-(2-hydroxy-2-phenylethyl)-2,5-pyrrolidinedione
68239-22-5

N-(2-hydroxy-2-phenylethyl)-2,5-pyrrolidinedione

Conditions
Conditions Yield
With chromium dichloride; lithium iodide; In tetrahydrofuran; at 50 ℃; for 6h;
84%
Succinimide
123-56-8,89963-74-6

Succinimide

styrene oxide
96-09-3

styrene oxide

N-(2-hydroxy-2-phenylethyl)-2,5-pyrrolidinedione
68239-22-5

N-(2-hydroxy-2-phenylethyl)-2,5-pyrrolidinedione

Conditions
Conditions Yield
With sodium hydroxide; water; at 150 - 160 ℃;
With pyridine; butan-1-ol;
With sodium; In ethanol; for 18h; Heating;
13.0 g
With N,N-dimethyl-formamide;

68239-22-5 Upstream products

  • 123-56-8
    123-56-8

    Succinimide

  • 96-09-3
    96-09-3

    styrene oxide

  • 54553-14-9
    54553-14-9

    succinic acid N-(chloromethyl)imide

  • 100-52-7
    100-52-7

    benzaldehyde

68239-22-5 Downstream products

  • 106272-54-2
    106272-54-2

    N -(β-acetoxy-phenethyl)-succinimide

  • 99989-77-2
    99989-77-2

    N -(4-nitro-β-nitryloxy-phenethyl)-succinimide

  • 7568-93-6
    7568-93-6

    2-Amino-1-phenylethanol

  • 120542-02-1
    120542-02-1

    N-[(E)-2-phenylvinyl]succinimide

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