Welcome to LookChem.com Sign In|Join Free
  • or
Tri(1-naphthyl)phosphine, when incorporated into gold(I) complexes, demonstrates high selectivity against ovarian carcinoma cells (A2780) while exhibiting minimal toxicity to normal human fibroblasts, making it a promising ligand for developing targeted anticancer therapies. Its role in enhancing the biological activity of gold(I) complexes underscores its potential as an alternative to conventional cisplatin-based treatments, particularly for ovarian cancer.

3411-48-1

Post Buying Request

3411-48-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

3411-48-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3411-48-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,1 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3411-48:
(6*3)+(5*4)+(4*1)+(3*1)+(2*4)+(1*8)=61
61 % 10 = 1
So 3411-48-1 is a valid CAS Registry Number.
InChI:InChI=1/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

3411-48-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (42304)  Tri(1-naphthyl)phosphine, 97%   

  • 3411-48-1

  • 0.5g

  • 281.0CNY

  • Detail
  • Alfa Aesar

  • (42304)  Tri(1-naphthyl)phosphine, 97%   

  • 3411-48-1

  • 2g

  • 901.0CNY

  • Detail
  • Alfa Aesar

  • (42304)  Tri(1-naphthyl)phosphine, 97%   

  • 3411-48-1

  • 10g

  • 2244.0CNY

  • Detail
  • Alfa Aesar

  • (42304)  Tri(1-naphthyl)phosphine, 97%   

  • 3411-48-1

  • 50g

  • 6427.0CNY

  • Detail
  • Aldrich

  • (667218)  Tri-1-naphthylphosphine  97%

  • 3411-48-1

  • 667218-1G

  • 535.86CNY

  • Detail
  • Aldrich

  • (667218)  Tri-1-naphthylphosphine  97%

  • 3411-48-1

  • 667218-5G

  • 1,751.49CNY

  • Detail

3411-48-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name trinaphthalen-1-ylphosphane

1.2 Other means of identification

Product number -
Other names Tri(naphthalen-1-yl)phosphine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3411-48-1 SDS

3411-48-1Relevant academic research and scientific papers

The reaction of red phosphorus with 1-bromonaphthalene in the KOH-DMSO system: Synthesis of tri(1-naphthyl)phosphane

Kuimov, Vladimir A.,Malysheva, Svetlana F.,Gusarova, Nina K.,Vakul'Skaya, Tamara I.,Khutsishvili, Spartak S.,Trofimov, Boris A.

, p. 198 - 203 (2011)

Red phosphorus reacts with 1-bromonaphthalene in the KOH-DMSO system upon heating (47-70°C, 3 h) to give tri(1-naphthyl)phosphane in 10% yield. Microwave activation (600 W, 6 min) of the reaction affords the above-mentioned phosphane in 25% yield.

Reaction of 1-bromonaphthalene with PH3 in the t-BuOK/DMSO system: PCl3-free synthesis of di(1-naphthyl)phosphine and its oxide

Kuimov, Vladimir A.,Matveeva, Elena A.,Khutsishvili, Spartak S.,Vakul'skaya, Tamara I.,Sinegovskaya, Lidiya M.,Malysheva, Svetlana F.,Gusarova, Nina K.,Trofimov, Boris A.

, p. 4723 - 4729 (2017/07/17)

The phosphine, generated together with hydrogen from red phosphorus and aqueous KOH, reacts with 1-bromonaphthalene in the t-BuOK/DMSO system under mild conditions (70 °C, atmospheric pressure) to give di(1-naphthyl)phosphine, which is easily oxidized in the presence of air to afford di(1-naphthyl)phosphine oxide in 45% preparative yield. Tri(1-naphthyl)phosphine and naphthalene are also formed in the reaction in 23 and 27% yield, respectively. According to ESR and UV data, the studied phosphination of 1-bromonaphthalene involves a single electron transfer process.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 3411-48-1