Cas no 5351-90-6 (Salicylic Aldehyde Thiosemicarbazone)

Salicylic Aldehyde Thiosemicarbazone structure
5351-90-6 structure
Product Name:Salicylic Aldehyde Thiosemicarbazone
CAS No:5351-90-6
MF:C8H9N3OS
MW:195.24156
CID:1586603
PubChem ID:135423926
Update Time:2024-11-02

Salicylic Aldehyde Thiosemicarbazone Chemical and Physical Properties

Names and Identifiers

    • Salicylic aldehyde thiosemicarbazone
    • N'-Salicylidenemercaptoformamide hydrazone
    • [H2-(Sal-tsc)]
    • 2-[(2-Hydroxyphenyl)methylene]hydrazinecarbothioamide, 2-Hydroxybenzaldehyde thiosemicarbazone, o-Hydroxybenzaldehyde thiosemicarbazone
    • 2-(2-hydroxybenzylidene)hydrazinecarbothioamide
    • SALICYLALDEHYDE THIOSEMICARBAZONE 95
    • Salicylaldehyde monothiosemicarbazone
    • 2-Hydroxybenzaldehyde [(mercapto)(amino)methylene]hydrazone
    • 2-formyl-(2-hydroxybenzene) thiosemicarbazone
    • 2'-hydroxybenzaldehyde-thiosemicarbazone
    • 2-[(2-hydroxyphenyl)methylene]hydrazinecarbothioamine
    • 1-(2-Hydroxybenzylidene)thiosemicarbazide
    • 1-Salicylidenethiosemicarbazide
    • 2-(hydroxybenzylidene)thiosemicarbazone
    • Salicylaldehyde thioseMicarbazone
    • (2E)-2-(2-hydroxybenzylidene)hydrazinecarbothioamide
    • WLN: SUYZMNU1R BQ
    • AKOS001267718
    • NSC 201642
    • Hydrazinecarbothioamide, 2-((2-hydroxyphenyl)methylene)-
    • (E)-2-(2-hydroxybenzylidene)hydrazinecarbothioamide
    • CS-0112105
    • NSC 733
    • Salicylaldehydthiosemicarbazon
    • Hydrazinecarbothioamide, 2-[(2-hydroxyphenyl)methylene]-, (2E)-
    • 2-(2-Hydroxybenzylidene)hydrazine-1-carbothioamide
    • Hydrazinecarbothioamide, 2-[(2-hydroxyphenyl)methylene]-
    • NSC733
    • 5351-90-6
    • NSC201642
    • NCGC00246425-01
    • SALICYLALDEHYDE THIOSEMICARBAZONE 95
    • Z49561499
    • NSC-733
    • OHNSRYBTSVDDKA-BJMVGYQFSA-N
    • HMS1651J13
    • MFCD00188550
    • [(E)-(2-hydroxyphenyl)methylideneamino]thiourea
    • CHEMBL242112
    • Salicylaldehyde thiosemicarbazone, 95%
    • AB01209855-01
    • STK864437
    • 17149-00-7
    • o-Hydroxybenzaldehyde thiosemicarbazone
    • SMR000414062
    • Salicylaldehyde, thiosemicarbazone
    • MLS000777668
    • Salicyaldehyde Thiosemicarbazone
    • F0777-0561
    • NSC-201642
    • AI3-22965
    • SCHEMBL3072985
    • [(E)-(2-hydroxyphenyl)methyleneamino]thiourea
    • Salicylic Aldehyde Thiosemicarbazone
    • Inchi: InChI=1S/C8H9N3OS/c9-8(13)11-10-5-6-3-1-2-4-7(6)12/h1-5,12H,(H3,9,11,13)/b10-5+
    • InChI Key: OHNSRYBTSVDDKA-BJMVGYQFSA-N
    • SMILES: NC(=S)N\N=C\c1ccccc1O

Computed Properties

  • Exact Mass: 195.04677
  • Monoisotopic Mass: 195.04663309g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 2
  • Complexity: 208
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 1
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 0.8
  • Topological Polar Surface Area: 103?2

Experimental Properties

  • Melting Point: >230?°C
  • PSA: 67.15
  • LogP: 1.65050

Salicylic Aldehyde Thiosemicarbazone Security Information

  • WGK Germany:3
  • RTECS:VN6125000

Salicylic Aldehyde Thiosemicarbazone Pricemore >>

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Salicylic Aldehyde Thiosemicarbazone Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Nickel acetate Solvents: Methanol ;  50 - 60 min, 50 - 55 °C; cooled
Reference
Synthesis and antimicrobial activity of sulfanylamide-containing copper(II) and nickel(II) salicylidenethiosemicarbazidates
Gulya, A. P.; et al, Pharmaceutical Chemistry Journal, 2007, 41(11), 596-599

Salicylic Aldehyde Thiosemicarbazone Raw materials

Salicylic Aldehyde Thiosemicarbazone Preparation Products

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