Benzophenone hydrazone

Benzophenone hydrazone
  • CAS No.:5350-57-2
Other grades of this product :
Benzophenone hydrazone Basic information
Synthesis
Product Name:Benzophenone hydrazone
Synonyms:3-iodo-N-[[2-[4-(2-methyl-1-oxopropyl)-1-piperazinyl]anilino]-sulfanylidenemethyl]benzamide;Ht--103 Benzophenonehydrazone (Bph);BENZOPHENONE HYDRAZONE;BENZOPHENONE HYDROZONE;Methanone, diphenyl-, hydrazone;Benzophenone hydrazone, 98+%;Benzophenone hydrazo;Di(phenyl)methylidenehydrazine
CAS:5350-57-2
MF:C13H12N2
MW:196.25
EINECS:226-321-8
Product Categories:Pharmaceutical Intermediates;Aromatic Hydrazides, Hydrazines, Hydrazones and Oximes;Phenylhydrazine;Heterocyclic Compounds;bc0001;5350-57-2
Mol File:5350-57-2.mol
Benzophenone hydrazone Chemical Properties
Melting point 95-98 °C (lit.)
Boiling point 225-230 °C/55 mmHg (lit.)
density 1.1
refractive index 1.5014 (estimate)
Fp 146°C
storage temp. 2-8°C
solubility Soluble in ether, benzene, chloroform and other organic solvents.
pka1.44±0.70(Predicted)
form Crystalline Needles or Crystalline Powder
color White to yellow
BRN 1910177
InChIKeyQYCSNMDOZNUZIT-UHFFFAOYSA-N
CAS DataBase Reference5350-57-2(CAS DataBase Reference)
NIST Chemistry ReferenceMethanone, diphenyl-, hydrazone(5350-57-2)
EPA Substance Registry SystemMethanone, diphenyl-, hydrazone (5350-57-2)
Safety Information
Hazard Codes 
Risk Statements 
Safety Statements 
WGK Germany 3
RTECS PC4954487
TSCA Yes
HS Code 29280090
MSDS Information
ProviderLanguage
Benzophenone hydrazone English
SigmaAldrich English
ACROS English
ALFA English
Benzophenone hydrazone Usage And Synthesis
SynthesisBenzophenone hydrazone was synthesised by Benzophenone and hydrazine hydrate stirred in ionic liquid for 0.5-6h at 0~140℃.
Chemical Propertieswhite to light yellow crystal powde
UsesAn important compound in organic photochemistry and perfumery as well as in organic synthesis. Used in the antibiotics synthesis of 6-APA and 7-ACA of the carboxyl protecting groups and other organic compounds. Used as organic pigment and medical intermediate. It is used as a photoinitiator of UV-curing applications in inks, adhesive, coatings and optical fiber.
Synthesis Reference(s)Journal of the American Chemical Society, 72, p. 2890, 1950 DOI: 10.1021/ja01163a024Organic Syntheses, Coll. Vol. 3, p. 351, 1955

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