Benzoylacetonitrile

Benzoylacetonitrile
  • CAS No.:614-16-4
Other grades of this product :
Benzoylacetonitrile Basic information
Product Name:Benzoylacetonitrile
Synonyms:BENZOYLACETONITRILE;BETA-OXOHYDROCINNAMONITRILE;AKOS B029579;AKOS 92208;ALPHA-CYANOACETOPHENONE;AKOS BB-9543;3-OXO-3-PHENYL-PROPIONITRILE;3-OXO-3-PHENYLPROPANENITRILE
CAS:614-16-4
MF:C9H7NO
MW:145.16
EINECS:210-369-1
Product Categories:Pyrazoles;Aromatic Nitriles;Aromatics;Miscellaneous Reagents
Mol File:614-16-4.mol
Benzoylacetonitrile Chemical Properties
Melting point 82-83 °C (lit.)
Boiling point 160 °C/10 mmHg (lit.)
density 1.1555 (rough estimate)
refractive index 1.4500 (estimate)
Fp 159-160°C/10mm
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form Solid
pka7.78±0.10(Predicted)
color Yellow to Dark Beige
Water Solubility slightly soluble
BRN 386745
Exposure limitsNIOSH: IDLH 25 mg/m3
InChIKeyZJRCIQAMTAINCB-UHFFFAOYSA-N
CAS DataBase Reference614-16-4(CAS DataBase Reference)
NIST Chemistry Reference«alpha»-Cyanoacetophenone(614-16-4)
EPA Substance Registry SystemBenzenepropanenitrile, .beta.-oxo- (614-16-4)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 20/21/22-36/37/38
Safety Statements 26-36-36/37/39-22
RIDADR 3276
WGK Germany 3
Hazard Note Harmful/Irritant
TSCA Yes
HazardClass IRRITANT
PackingGroup III
HS Code 29269090
MSDS Information
ProviderLanguage
Cyanoacetophenone English
ACROS English
SigmaAldrich English
ALFA English
Benzoylacetonitrile Usage And Synthesis
Chemical PropertiesLIGHT YELLOW TO YELLOW-BROWN CRYSTALLINE POWDER
UsesBenzoylacetonitrile can be used as a building block for the preparation of 4H-pyrans, 2-pyridones, furans and carbocyclics
UsesBenzoylacetonitrile is used to produce 2-benzoyl-3-furan-2-yl-acrylonitrile. It is also used in the synthesis of substituted naphtho[1,8-bc]pyrans and as building block in the preparation of 4H-pyrans, 2-pyridones, furans and carbocyclics. It is an active methylene compound, useful in heterocyclic synthesis, e.g. polyfunctional pyridines and pyrimidines.
Synthesis Reference(s)The Journal of Organic Chemistry, 54, p. 4229, 1989 DOI: 10.1021/jo00278a047Synthesis, p. 308, 1983Tetrahedron, 49, p. 5091, 1993 DOI: 10.1016/S0040-4020(01)81874-3

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