86-96-4

  • Product Name:Benzoyleneurea
  • Molecular Formula:C8H6N2O2
  • Purity:99%
  • Molecular Weight:162.148
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Product Details;

CasNo: 86-96-4

Molecular Formula: C8H6N2O2

Appearance: white to light pink fluffy powder

factory and supplier 86-96-4 Benzoyleneurea in stock

  • Molecular Formula:C8H6N2O2
  • Molecular Weight:162.148
  • Appearance/Colour:white to light pink fluffy powder 
  • Vapor Pressure:0.015mmHg at 25°C 
  • Melting Point:300 °C 
  • Refractive Index:1.565 
  • Boiling Point:491.9oC at 760 mmHg 
  • PKA:11.12±0.20(Predicted) 
  • Flash Point:119.681°C 
  • PSA:65.72000 
  • Density:1.337 g/cm3 
  • LogP:0.21640 

Benzoyleneurea(Cas 86-96-4) Usage

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 21, p. 5, 1984 DOI: 10.1002/jhet.5570210102Organic Syntheses, Coll. Vol. 2, p. 79, 1943

InChI:InChI=1/C8H8N2O/c11-8-9-5-6-3-1-2-4-7(6)10-8/h1-4H,5H2,(H2,9,10,11)

86-96-4 Relevant articles

Synthesis of quinazoline-2,4(1H,3H)-dione from carbon dioxide and 2-aminobenzonitrile using mesoporous smectites incorporating alkali hydroxide

Fujita, Shin-Ichiro,Tanaka, Masahiro,Arai, Masahiko

, p. 1563 - 1569 (2014)

A series of magnesium containing mesopor...

Synthetic approaches, functionalization and therapeutic potential of quinazoline and quinazolinone skeletons: The advances continue

Khan, Imtiaz,Ibrar, Aliya,Ahmed, Waqas,Saeed, Aamer

, p. 124 - 169 (2015)

The presence of N-heterocycles as an ess...

-

Lange,Sheibley

, p. 79 (1943)

-

ZIF-8-Nanocrystalline Zirconosilicate Integrated Porous Material for the Activation and Utilization of CO2 in Insertion Reactions

Srivastava, Diksha,Rani, Poonam,Srivastava, Rajendra

, p. 1132 - 1139 (2020)

The conversion of CO2 to useful chemical...

Delineating the Mechanism of Ionic Liquids in the Synthesis of Quinazoline-2,4(1H,3H)-dione from 2-Aminobenzonitrile and CO2

Hulla, Martin,Chamam, Sami M. A.,Laurenczy, Gabor,Das, Shoubhik,Dyson, Paul J.

, p. 10559 - 10563 (2017)

Ionic liquids (ILs) are versatile solven...

-

Hegarty,Bruice

, p. 4924 (1969)

-

UNEXPECTED FORMATION OF 2,4-QUINAZOLINEDIONE IN THE REACTION OF α-CYANO-β-DIMETHYLAMINOCROTONAMIDE WITH ETHYL ANTHRANILATE

Yalysheva, N. Z.,Granik, V. G.

, p. 1186 (1984)

-

Design, synthesis, in silico ADMET, docking, and antiproliferative evaluations of [1,2,4]triazolo[4,3-c]quinazolines as classical DNA intercalators

Alesawy, Mohamed S.,Eissa, Ibrahim H.,El-Adl, Khaled,Ibrahim, Mohamed-Kamal

, (2022/01/13)

Eleven novel [1,2,4]triazolo[4,3-c]quina...

Synthesis, biological evaluation, and molecular docking of new series of antitumor and apoptosis inducers designed as VEGFR-2 inhibitors

Abdallah, Abdallah E.,Abo-Saif, Mariam A.,Al Ward, Maged Mohammed Saleh,Alesawy, Mohamed S.,Eissa, Sally I.,El-Feky, Ola A.,El-Zahabi, Mohamed Ayman,Elkaeed, Eslam B.,Mabrouk, Reda R.,Mehany, Ahmed B. M.

, p. 573 - 591 (2022/01/20)

Based on quinazoline, quinoxaline, and n...

[TBDH][HFIP] ionic liquid catalyzed synthesis of quinazoline-2,4(1H,3H)-diones in the presence of ambient temperature and pressure

Phatake, Vishal V.,Gokhale, Tejas A.,Bhanage, Bhalchandra M.

, (2021/07/28)

The utilization of carbon dioxide under ...

Synthesis of acyclic nucleoside phosphonates targeting flavin-dependent thymidylate synthase in Mycobacterium tuberculosis

Agrofoglio, Luigi A.,Becker, Hubert F.,Biteau, Nicolas G.,Lambry, Jean-Christophe,Myllykallio, Hannu,Roy, Vincent

, (2021/08/16)

Flavin-Dependent Thymidylate Synthase (F...

86-96-4 Process route

2-thioxo-2,3-dihydro-1H-quinazolin-4-one
13906-09-7

2-thioxo-2,3-dihydro-1H-quinazolin-4-one

4-Hydroxyquinazoline
491-36-1

4-Hydroxyquinazoline

1,2,3,4-tetrahydro-quinazoline-2,4-dione
86-96-4

1,2,3,4-tetrahydro-quinazoline-2,4-dione

Conditions
Conditions Yield
With ozone; In water; acetic acid; at 25 ℃; for 1h;
13%
75%
2-mercapto-3H-quinazolin-4-one
13906-09-7

2-mercapto-3H-quinazolin-4-one

4-Hydroxyquinazoline
491-36-1

4-Hydroxyquinazoline

1,2,3,4-tetrahydro-quinazoline-2,4-dione
86-96-4

1,2,3,4-tetrahydro-quinazoline-2,4-dione

Conditions
Conditions Yield
With ozone; In water; acetic acid; at 25 ℃; for 1h;
13%
75%

86-96-4 Upstream products

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    491-36-1

    4-Hydroxyquinazoline

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    (E)-3-iminoindolin-2-one

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    phthalamide

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    57212-70-1

    N-(mesyloxy)phthalimide

86-96-4 Downstream products

  • 607-19-2
    607-19-2

    3-methyl-2,4(1H,3H)-quinazolinedione

  • 1013-01-0
    1013-01-0

    1,3-dimethyl-1H-quinazoline-2,4-dione

  • 84587-34-8
    84587-34-8

    1,3-dibenzoylquinazoline-2,4-dione

  • 2217-26-7
    2217-26-7

    3-ethyl-1H-quinazoline-2,4-dione

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