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1,3-BIS(DICYCLOPENTYLPHOSPHINOMETHYL)BENZENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

255874-48-7

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255874-48-7 Usage

Uses

Catalyst for intermediate of Heck reactions

Check Digit Verification of cas no

The CAS Registry Mumber 255874-48-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,5,8,7 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 255874-48:
(8*2)+(7*5)+(6*5)+(5*8)+(4*7)+(3*4)+(2*4)+(1*8)=177
177 % 10 = 7
So 255874-48-7 is a valid CAS Registry Number.

255874-48-7 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Detail
  • Aldrich

  • (680451)  [1,3-Phenylenebis(methylene)]bis(dicyclopentylphosphine)  95%

  • 255874-48-7

  • 680451-100MG

  • 451.62CNY

  • Detail
  • Aldrich

  • (680451)  [1,3-Phenylenebis(methylene)]bis(dicyclopentylphosphine)  95%

  • 255874-48-7

  • 680451-500MG

  • 1,726.92CNY

  • Detail

255874-48-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name dicyclopentyl-[[3-(dicyclopentylphosphanylmethyl)phenyl]methyl]phosphane

1.2 Other means of identification

Product number -
Other names -

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:255874-48-7 SDS

255874-48-7Upstream product

255874-48-7Downstream Products

255874-48-7Relevant academic research and scientific papers

Heck reactions: A caveat on the use of palladium(II) PCP-type catalysts

Kiewel, Kurt,Liu, Yunshan,Bergbreiter, David E.,Sulikowski, Gary A.

, p. 8945 - 8948 (2007/10/03)

A PCP-type catalyst was prepared and examined within the context of intramolecular Heck reactions. A substrate possessing a 1,4-diene system effectively poisoned the PCP catalyst leading to no reaction. This behavior contrasts with the typical palladium(0) catalyst system.

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