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2-Phenyl-1,3-indanedione

CAS
92-43-2
Catalog Number
ACM92432
Category
Other Products
Molecular Weight
162.18800
Molecular Formula
C9H10N2O

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Specification

Synonyms
PYRAZOLIDONE A; graphidone; B PHENIDONE B; 1-hydro-2-phenyl-pyrazol-5-one; 1-phenyl-3-pyrazolidinone; PHENIDONE A; 1-phenyl-pyrazolidin-3-on; phenitone; 1-phenyl-3-pyrazolidone; S PHENIDONE S; Fenidon; A PHENIDONE A; 1-phenyl-1H-pyrazolidin-3-one; N-pheny
IUPAC Name
Phenidone
Boiling Point
304.1ºC at 760 mmHg
Melting Point
119-123ºC
Density
1.188 g/cm³
Appearance
light beige powder or crystals
Exact Mass
162.07900
Hazard Statements
Xn:Harmful;N:Dangerousfortheenvironment;
Packing Group
III
Safety Description
S61
Stability
Stable, but light sensitive. Incompatible with strong acids, strong oxidizing agents, strong bases.
WGK Germany
2
What is the molecular formula of 2-Phenyl-1,3-indanedione?

The molecular formula of 2-Phenyl-1,3-indanedione is C15H10O2.

What is the molecular weight of 2-Phenyl-1,3-indanedione?

The molecular weight of 2-Phenyl-1,3-indanedione is 222.24 g/mol.

What is the IUPAC name of 2-Phenyl-1,3-indanedione?

The IUPAC name of 2-Phenyl-1,3-indanedione is 2-phenylindene-1,3-dione.

What is the CAS number of 2-Phenyl-1,3-indanedione?

The CAS number of 2-Phenyl-1,3-indanedione is 83-12-5.

What is the EC number of 2-Phenyl-1,3-indanedione?

The EC number of 2-Phenyl-1,3-indanedione is 201-454-4.

What is the ChEMBL ID of 2-Phenyl-1,3-indanedione?

The ChEMBL ID of 2-Phenyl-1,3-indanedione is CHEMBL711.

What is the UNII of 2-Phenyl-1,3-indanedione?

The UNII of 2-Phenyl-1,3-indanedione is 5M7Y6274ZE.

What is the InChIKey of 2-Phenyl-1,3-indanedione?

The InChIKey of 2-Phenyl-1,3-indanedione is NFBAXHOPROOJAW-UHFFFAOYSA-N.

What is the role of 2-Phenyl-1,3-indanedione?

2-Phenyl-1,3-indanedione has a role as an anticoagulant.

How does 2-Phenyl-1,3-indanedione work as an anticoagulant?

2-Phenyl-1,3-indanedione inhibits vitamin K reductase, resulting in the depletion of the reduced form of vitamin K (vitamin KH2). This limits the gamma-carboxylation and subsequent activation of the vitamin K-dependent coagulant proteins, leading to a decrease in prothrombin levels and a reduction in the thrombogenicity of clots.

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