Welcome to LookChem.com Sign In|Join Free
  • or
Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)]palladium(II), also known as P(t-Bu)3 Pd G2, is a second-generation (G2) precatalyst that contains a biphenyl-based ligand. It is known for its ability to participate in various palladium-catalyzed cross-coupling reactions, C-C, C-N, and C-O bond formation reactions, as well as Suzuki-Miyaura coupling reactions. Chloro[(tri-tert-butylphosphine)-2-(2-aMinobiphenyl)]palladiuM(II) generates an active Pd catalyst at room temperature in the presence of weak phosphate or carbonate bases and has been proposed as an active catalyst for use in Stille reactions of aryl halides, such as bromides and chlorides.

1375325-71-5

Post Buying Request

1375325-71-5 Suppliers

Recommended suppliers

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

1375325-71-5 Usage

Uses

Used in Chemical Synthesis:
Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)]palladium(II) is used as a catalyst for the synthesis of sterically hindered biaryls (tetra-ortho-substituted) via cross-coupling reactions of aryl chlorides. It is particularly effective in Stille cross-coupling reactions of aryl chlorides, which are essential for the synthesis of various organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)]palladium(II) is used as a catalyst for the synthesis of chloropeptin I, an important compound in the development of new antibiotics, via Stille cross-coupling reaction.
Used in Organic Chemistry Research:
Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)]palladium(II) is used as a catalyst in Heck and Negishi cross-coupling reactions, which are crucial for the formation of C-C, C-N, and C-O bonds in organic chemistry. These reactions are essential for the synthesis of complex organic molecules and the development of new materials and pharmaceuticals.
Overall, Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)]palladium(II) is a versatile and efficient catalyst with a wide range of applications in chemical synthesis, pharmaceutical industry, and organic chemistry research. Its ability to facilitate various cross-coupling reactions and bond formations makes it a valuable tool for the development of new compounds and materials.

Physical Form

Yellow powder

Reaction

Catalyst for the Suzuki Coupling of brominated 2,1-borazaronaphthalenes and potassium organotrifluoroborates.

Check Digit Verification of cas no

The CAS Registry Mumber 1375325-71-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,5,3,2 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1375325-71:
(9*1)+(8*3)+(7*7)+(6*5)+(5*3)+(4*2)+(3*5)+(2*7)+(1*1)=165
165 % 10 = 5
So 1375325-71-5 is a valid CAS Registry Number.

1375325-71-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)]palladium(II)

1.2 Other means of identification

Product number -
Other names 4,4,4-Trifluoroacetoacetic Acid Ethyl Ester

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:1375325-71-5 SDS

1375325-71-5Upstream product

1375325-71-5Downstream Products

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 1375325-71-5