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278971

Sigma-Aldrich

Diphenyl N-cyanocarbonimidate

97%

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About This Item

Linear Formula:
NCN=C(OC6H5)2
CAS Number:
79463-77-7
Molecular Weight:
238.24
Beilstein:
4254248
MDL number:
MFCD00010380
UNSPSC Code:
12352100
PubChem Substance ID:
24856845
NACRES:
NA.22

Quality Level

200

Assay

97%

form

solid

mp

155-158 °C (lit.)

SMILES string

N#C\N=C(/Oc1ccccc1)Oc2ccccc2

InChI

1S/C14H10N2O2/c15-11-16-14(17-12-7-3-1-4-8-12)18-13-9-5-2-6-10-13/h1-10H

InChI key

SLIKWVTWIGHFJE-UHFFFAOYSA-N

Gene Information

human ... EPHX2(2053)
mouse ... Ephx2(13850)

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Related Categories

Application

Diphenyl N-cyanocarbonimidate has been used in the preparation of:
  • N-substituted 2-amino-4H-3,1-benzoxazines
  • cyanoguanidine derivatives
  • oxadiazoles

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H318,H412

Hazard Classifications

Aquatic Chronic 3 - Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Tetrahedron Letters, 48, 2733-2733 (2007)
4H-3, 1-Benzoxazines, Their Salts and Dihydro Derivatives.(Review).
Gromachevskaya EV, et al.
Chemistry of Heterocyclic Compounds, 39(2), 137-155 (2003)
Bassem Sadek et al.
Molecules (Basel, Switzerland), 18(11), 14186-14202 (2013-11-20)
Premedication with a combination of histamine H₁ receptor (H₁R) and H₂ receptor (H₂R) antagonists has been suggested as a prophylactic principle, for instance, in anaesthesia and surgery. Aiming at pharmacological hybrids combining H₁R and H₂R antagonistic activity, a series of

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