O-TOLUAMIDE
O-TOLUAMIDE
  • CAS No.:527-85-5
Other grades of this product :
O-TOLUAMIDE Basic information
Product Name:O-TOLUAMIDE
Synonyms:2-METHYLBENZAMIDE;2-TOLUAMIDE;2-methyl-benzamid;Formyl-o-toluidine;o-Methylbenzamide;o-Toluic amide;o-Tolylamide;Benzamide, 2-methyl- (9CI)
CAS:527-85-5
MF:C8H9NO
MW:135.16
EINECS:208-427-6
Product Categories:Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;AMIDE
Mol File:527-85-5.mol
O-TOLUAMIDE Chemical Properties
Melting point 141-142 °C (lit.)
Boiling point 248.86°C (rough estimate)
density 1.086
refractive index 1.5589 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility alcohol: very soluble(lit.)
pka16.01±0.50(Predicted)
Merck 13,9606
CAS DataBase Reference527-85-5
EPA Substance Registry Systemo-Toluamide (527-85-5)
Safety Information
Hazard Codes Xn
Risk Statements 22
WGK Germany 3
HS Code 2924297099
MSDS Information
O-TOLUAMIDE Usage And Synthesis
Uses2-Methylbenzamide (o-Toluamide) has been used in total synthesis of phenolic protoberberine alkaloid, cerasonine.
Synthesis Reference(s)Organic Syntheses, Coll. Vol. 2, p. 586, 1943The Journal of Organic Chemistry, 57, p. 2700, 1992 DOI: 10.1021/jo00035a030
General DescriptionWhite powder.
Air & Water ReactionsInsoluble in water.
Reactivity ProfileO-TOLUAMIDE is an amide. Amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).
Health HazardACUTE/CHRONIC HAZARDS: O-TOLUAMIDE may react violently if exposed to open flame; it should be isolated from all sources of ignition.
Fire HazardFlash point data for O-TOLUAMIDE are not available, however O-TOLUAMIDE is probably combustible.
Purification MethodsCrystallise o-toluamide from hot water (10mL/g) and dry in air. [Noller Org Synth Coll Vol II 586 1943, Beilstein 9 H 465, 9 II 319, 9 III 2304.]

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