• Product NameN-Hydroxyethylphthalimide
  • CasNo. 3891-07-4
  • MFC10H9NO3
  • MW191.186
  • Purity
  • Appearancewhite crystalline powder
  • Packing
  • Contact usInquiry

Product Details

CasNo: 3891-07-4

MF: C10H9NO3

Appearance: white crystalline powder

Trustworthy Factory Supply 3891-07-4 with Lowest Price, Factory Sells N-Hydroxyethylphthalimide

  • Molecular Formula:C10H9NO3
  • Molecular Weight:191.186
  • Appearance/Colour:white crystalline powder 
  • Vapor Pressure:1.06E-05mmHg at 25°C 
  • Melting Point:126-129 °C 
  • Refractive Index:1.622 
  • Boiling Point:356.5 °C at 760 mmHg 
  • PKA:14.40±0.10(Predicted) 
  • Flash Point:169.4 °C 
  • PSA:57.61000 
  • Density:1.388 g/cm3 
  • LogP:0.21280 

N-Hydroxyethylphthalimide(Cas 3891-07-4) Usage

Synthesis Reference(s)

Organic Syntheses, Coll. Vol. 4, p. 106, 1963The Journal of Organic Chemistry, 24, p. 1122, 1959 DOI: 10.1021/jo01090a601

General Description

N-(2-Hydroxyethyl)phthalimide is the precursor for chloromethyl ethers used in the synthesis of purine acyclic nucleosides.

InChI:InChI=1/C10H9NO3/c12-6-5-11-9(13)7-3-1-2-4-8(7)10(11)14/h1-4,12H,5-6H2

3891-07-4 Relevant articles

Microgels as Matrices for Molecular Receptor and Reactive Sites: Synthesis and Reactivity of Cavities possessing Amino-functions

Hopkins, Andrew,Williams, Andrew

, p. 891 - 896 (1983)

Non-fluxional polymeric particles, micro...

Activities of 2-phthalimidethanol and 2-phthalimidethyl nitrate, phthalimide analogs devoid of the glutarimide moiety, in experimental models of inflammatory pain and edema

Godin, Adriana M.,Araújo, Débora P.,Menezes, Raquel R.,Brito, Ana Mercy S.,Melo, Ivo S.F.,Coura, Giovanna M.E.,Soares, Darly G.,Bastos, Leandro F.S.,Amaral, Flávio A.,Ribeiro, Lucas S.,Boff, Daiane,Santos, Julliana R.A.,Santos, Daniel A.,Teixeira, Mauro M.,De Fátima, ?ngelo,Machado, Renes R.,Coelho, Márcio M.

, p. 291 - 298 (2014)

The reintroduction of thalidomide in the...

-

Wenker

, p. 422 (1937)

-

-

Rose

, (1948)

-

Facile synthesis of indolizinoindolone, indolylepoxypyrrolooxazole, indolylpyrrolooxazolone and isoindolopyrazinoindolone heterocycles from indole and imide derivatives

Argade, Narshinha P.,Shelar, Santosh V.

, p. 6160 - 6169 (2021/07/21)

Chemo-, regio- and diastereoselective co...

Novel synthesis method of N-hydroxyethyl phthalimide

-

Paragraph 0014-0023, (2021/09/04)

The invention discloses a novel synthesi...

FLUORINATED BENZO[F]BENZIMIDAZOL-4-9-DIONE IUM DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS THEREOF AND THEIR USE AS SURVIVIN SUPPRESSANTS

-

Paragraph 00176; 00178, (2020/09/30)

The present application relates to novel...

Synthesis method of 2-(phthalimido)ethanesulfonyl chloride

-

Paragraph 0033; 0034; 0037; 0038; 0041; 0042; 0045; 0046, (2019/03/28)

The invention discloses a synthesis meth...

3891-07-4 Process route

N-phthalimido-D,L-serine
65391-10-8

N-phthalimido-D,L-serine

N-methylphthalimide
550-44-7

N-methylphthalimide

N-vinylphthalimide
3485-84-5,26809-43-8

N-vinylphthalimide

N-(2-Hydroxyethyl)phthalimide
3891-07-4

N-(2-Hydroxyethyl)phthalimide

Conditions
Conditions Yield
In acetonitrile; for 10h; Irradiation;
75%
10%
(2S)-2-(1,3-dioxoisoindolin-2-yl)-3-hydroxypropanoic acid
29588-89-4

(2S)-2-(1,3-dioxoisoindolin-2-yl)-3-hydroxypropanoic acid

N-methylphthalimide
550-44-7

N-methylphthalimide

N-vinylphthalimide
3485-84-5,26809-43-8

N-vinylphthalimide

N-(2-Hydroxyethyl)phthalimide
3891-07-4

N-(2-Hydroxyethyl)phthalimide

Conditions
Conditions Yield
In acetonitrile; at 13 ℃; for 24h; Product distribution; Mechanism; Irradiation; effect of various solvents on product/yield distribution;
83 % Spectr.
9 % Spectr.
8 % Spectr.

3891-07-4 Upstream products

  • 75-21-8
    75-21-8

    oxirane

  • 136918-14-4
    136918-14-4

    phthalimide

  • 96-49-1
    96-49-1

    [1,3]-dioxolan-2-one

  • 85-44-9
    85-44-9

    phthalic anhydride

3891-07-4 Downstream products

  • 4537-76-2
    4537-76-2

    distearylphosphatidylethanolamine

  • 20255-95-2
    20255-95-2

    dimyristoylphosphatidylethanolamine

  • 5466-90-0
    5466-90-0

    2-(1,3(2H)-dioxo-1H-isoindol-2-yl)ethyl acetate

  • 6656-84-4
    6656-84-4

    2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethyl benzoate

Relevant Products