Tri(1-naphthyl)phosphine

Inquiry

Molecular Formula:

C30H21P

Molecular Weight:

412.47

CAS Number:

3411-48-1

Catalog Number:

3411-48-1

Product Information

Molecular Formula:

C30H21P

Molecular Weight:

412.47

Description

Tri(1-naphthyl)phosphine is a vital compound extensively used in the biomedical industry. It is primarily employed in the synthesis of various drugs and pharmaceutical compounds. With its unique chemical properties, Tri(1-naphthyl)phosphine contributes to the development of drugs targeting specific diseases and medical conditions, including cancer, inflammation, and neurological disorders.

Synonyms

TRI(1-NAPHTHYL)PHOSPHINE; TRIS(1-NAPHTHYL)PHOSPHINE; BARIUM ZIRCONIUM ISOPROPOXIDE, 10% W/V IN ISOPROPANOL; BARIUM ZIRCONIUM ISOPROPOXIDE, 10% W/V IN ISOPROPANOL, PACKA; Tri-(1-naphthyl)phosphin; Tri(1-naphthyl)phosphine, 96+%

IUPAC Name

trinaphthalen-1-ylphosphane

Canonical SMILES

C1=CC=C2C(=C1)C=CC=C2P(C3=CC=CC4=CC=CC=C43)C5=CC=CC6=CC=CC=C65

InChI

InChI=1S/C30H21P/c1-4-16-25-22(10-1)13-7-19-28(25)31(29-20-8-14-23-11-2-5-17-26(23)29)30-21-9-15-24-12-3-6-18-27(24)30/h1-21H

InChI Key

DMEUUKUNSVFYAA-UHFFFAOYSA-N

Boiling Point

599.4°C at 760 mmHg

Melting Point

265-268°C

Flash Point

Not applicable

Purity

95%

Appearance

White to tan solid

Safety Information

Hazards

H302

Computed Properties

XLogP3

8.4

Hydrogen Bond Donor Count

Hydrogen Bond Acceptor Count

Rotatable Bond Count

Exact Mass

412.138087668 g/mol

Monoisotopic Mass

412.138087668 g/mol

Topological Polar Surface Area

0Å²

Heavy Atom Count

Formal Charge

Complexity

504

Isotope Atom Count

Defined Atom Stereocenter Count

Undefined Atom Stereocenter Count

Defined Bond Stereocenter Count

Undefined Bond Stereocenter Count

Covalently-Bonded Unit Count

Compound Is Canonicalized

Yes

Patents

Publication Number	Title	Priority Date
CN-113372323-A	Method for synthesizing camptothecin compound intermediate under microwave and normal pressure	2021-05-13
CN-113224313-A	Metal organic phosphine frame glass modified metal negative current collector and preparation method thereof	2021-04-30
WO-2022025243-A1	Polycarbonate resin composition and molded item thereof	2020-07-31
EP-3945088-A1	Process for minimising the loss of activity in reaction steps carried out in circulation	2020-07-30
WO-2022022939-A1	Process for minimising the loss of activity in reaction steps carried out in circulation	2020-07-30
CN-113946098-A	Colored curable resin composition, color filter, and display device	2020-07-16
CN-113946100-A	Colored curable resin composition, color filter, and display device	2020-07-16
JP-2022018965-A	Color curable resin composition, color filter and display device	2020-07-16
JP-2022018966-A	Color curable resin composition, color filter and display device	2020-07-16
KR-20220009874-A	Coloring curable resin composition, color filter and display device	2020-07-16

Literatures

PMID	Publication Date	Title	Journal
22065702	2011-10-01	trans-Carbonyl-chloridobis[tris(naph-thalen-1-yl)-phosphane-κP]rhodium(I) acetone trisolvate	Acta crystallographica. Section E, Structure reports online
22059061	2011-09-01	Chloro-bis-(naphthalen-1-yl)phosphane	Acta crystallographica. Section E, Structure reports online

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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The dilution calculator equation

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

This equation is commonly abbreviated as: C₁V₁ = C₂V₂

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