Organic Chemicals

Benzoyl isothiocyanate

  • CAS:532-55-8
  • purity:99%
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Manufacturers supply cost-effective and customizable Benzoyl isothiocyanate 532-55-8

  • Molecular Formula: C8H5NOS
  • Molecular Weight: 163.2
  • Appearance/Colour: clear yellow to orange-brown liquid 
  • Vapor Pressure: 0.0201mmHg at 25°C 
  • Melting Point: 128 °C 
  • Refractive Index: n20/D 1.6354(lit.)  
  • Boiling Point: 251.7 °C at 760 mmHg 
  • Flash Point: 106 °C 
  • PSA: 61.52000 
  • Density: 1.214 g/cm3 
  • LogP: 1.92960 

Benzoyl isothiocyanate(Cas 532-55-8) Usage

Purification Methods

Distil the isothiocyanate over a small amount of P2O5, whereby the distillate crystallises in prisms. It is readily hydrolysed by H2O to give benzamide and benzoylurea, but with NH3 it gives benzoylurea m 210o which can be recrystallised from EtOH. [Hill & Degnan J Am Chem Soc 62 1595 1940, Terss & McEwen J Am Chem Soc 76 580 1954, Frank & Smith Org Synth Coll Vol III 735 1955, Beilstein 9 IV 777.]

InChI:InChI=1/C8H5NOS/c10-8(9-6-11)7-4-2-1-3-5-7/h1-5H

532-55-8 Relevant articles

Structural, spectral, optical and antimicrobial properties of synthesized 1-benzoyl-3-furan-2-ylmethyl-thiourea

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The interest in the present study pertai...

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Kuznetsov, A. I.,Serova, T. M.,Vladimirova, I. A.,Barri, U.,Ngi, Chan,Moskovkin, A. S.

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Hepatitis C virus serine protease: Synthesis of radioactive and stable isotope-labeled potent inhibitors

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The present study describes the synthesi...

Thiocarbamoylation of 1,3,3-trimethyl-3,4-dihydroisoquinolines with benzoyl isothiocyanate

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Characterization and Computational Studies of 2-(Benzamido)Thiazol-5-yl Benzoate

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2-(Benzamido)thiazolylbenzoate is synthe...

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Hepatitis C virus (HCV) serine protease ...

The synthesis of triazolothiadiazines and thiadiazoles from 1,2-bis-(4-amino-5-mercapto-1,2,4-triazol-3-yl)-ethanol and ethane

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The reaction of DL-malic and succinic ac...

Theoretical studies of molecular structure and vibrational spectra of O-ethyl benzoylthiocarbamate

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, p. 936 - 943 (2007)

O-Ethyl benzoylthiocarbamate has been sy...

Synthesis and intramolecular cyclization of N-acyl- and N-allyl-N'-(2-oxo-1,2-dihydro-pyridin-3-yl)thiourea

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The reaction of 3-amino-4,6-dimethylpyri...

Synthesis and characterization of copper(I) halide complexes with N-(2, 6-diisopropylphenyl)-N′-benzoylthiourea: Monomeric, dimeric, and cage structures

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2,4,6-Trimethylphenyl-3-benzoylthiourea ...

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Phthalazinone in heterocyclic synthesis: Synthesis of some s-triazole, s-triazolothiadiazine, s-triazolothiadiazine, and s-triazolothiadiazole derivatives as pharmaceutical interest

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1(2H)-Oxophthalazine-2-acetic acid ethyl...

DNA binding, DNA cleavage and HSA interaction of several metal complexes containing N-(2-hydroxyethyl)-N′-benzoylthiourea and 1,10-phenanthroline ligands

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, p. 903 - 916 (2016)

Abstract: Four novel ternary metal compl...

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Three different acyl thiourea derivative...

Synthesis, supramolecular structure, antimicrobial and plant-growth regulation activities of n-benzoylthiourea

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, p. 237 - 240 (2014)

N-Benzoylthiourea has been synthesized a...

1-Benzoyl-3-[(2-benzylsulfanyl)phenyl]thiourea

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In the title compound, C21H18N2OS2, a st...

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An efficient procedure for the preparati...

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Mononuclear copper(i) complexes of triphenylphosphine and: N, N ′-disubstituted thioureas as potential DNA binding chemotherapeutics

Khan, Syed Ishtiaq,Ahmad, Sajjad,Khan, Inayat Ali,Badshah, Amin,Rauf, Muhammad Khawar,Putejo, Jahangir Ali,Siddiq, Muhammad Nasir,Kausar, Samia,Altaf, Ataf Ali

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In this work, nine new mixed-ligand comp...

Electrochemical sensing of doxepin using acylthiourea-modified glassy carbon electrode

Bhuvanesh, N. S. P.,Biju, V. M.,Kalaiyarasi, A.,Karvembu, R.

, (2021/12/23)

Acylthiourea (ATU) compounds 4-(3-(furan...

532-55-8 Process route

phosphoryl-isothiocyanate
1858-25-9

phosphoryl-isothiocyanate

benzoyl chloride
98-88-4

benzoyl chloride

Benzoyl isothiocyanate
532-55-8

Benzoyl isothiocyanate

trichlorophosphate
10025-87-3,12599-09-6,63736-95-8,39380-77-3

trichlorophosphate

Conditions
Conditions Yield
1-benzoyl-3-phenylthiourea
4921-82-8

1-benzoyl-3-phenylthiourea

N-phenyl benzoyl amide
93-98-1,5705-51-1

N-phenyl benzoyl amide

benzamide
55-21-0,27208-38-4

benzamide

benzaldehyde
100-52-7

benzaldehyde

aniline
62-53-3

aniline

Benzoyl isothiocyanate
532-55-8

Benzoyl isothiocyanate

N,N-diphenylthiourea
102-08-9

N,N-diphenylthiourea

Conditions
Conditions Yield
With air; at 230 ℃; for 10h; Mechanism; Product distribution; further identificated products isolated; analogous reaction of other thiourea derivatives;

532-55-8 Upstream products

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    potassium thioacyanate

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    benzoyl chloride

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    lead(II) thiocyanate

  • 71-43-2
    71-43-2

    benzene

532-55-8 Downstream products

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    58415-38-6

    N-(piperidylthiocarbonyl)benzamide

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    4921-86-2

    N-benzoyl-N'-(2-pyridyl)thiourea

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    5461-34-7

    N1 -Benzoyl-N2 - <4-hydroxyphenyl> thiourea

  • 4921-84-0
    4921-84-0

    N-(naphthalen-1-ylcarbamothioyl)benzamide

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