Factory Price Monel 400 Seamless Tube & Pipe

Model NO.: Monel 400
Surface Treatment: Bright
Trademark: Taicheng
Transport Package: Plywood Case Lined with Foam or as Per Clients Req
Specification: 1-300
Origin: China
HS Code: 7507110000

Product Description


Monel 400 


Standard:ASTM B160 /162
Material:Ni200,Ni201,Monel,Inconel 
Dia.: 0.1~200mm 
ISO 9001:2008, ISO14001:2004 certificate.

 

We are manufacturer of non-ferrous mill products including Titanium,Nickel,Tantalum etc and has passed ISO 9001:2008 certification,so we are capable of supplying titanium mill products and nickel products like nickel wire,under ASTM B162/160,ASME,AMS,DIN,JIS etc with reliable quality and favourable price.

 

1>nickel bar

Item name

nickel bar

Standard

ASTM B160

Material

Ni200,Ni2001,Monel 400/k-500,600,Inconel 825 etc

Dia.

0.1~200mm

MOQ

10kg

Packaging

Plywood case lined with foam or as per clients request

Payment  terms

T/T or L/C at sight,western union

Leadtime

Within 10-25 days after deposit

Applications

Chemical Processing,Petrochemicals Industry, Oil Refineries, Pharmaceuticals, Fertilizers Plants, Sugar Mills, Textile etc

 

Factory Price Monel 400 Seamless Tube & Pipe


Factory Price Monel 400 Seamless Tube & Pipe

CONTACT INFORMATION-------------------
Sarah           (sales manger)
MOB            : 0086 13400006895
TEL/FAX     :0086-
510-88222973

Please feel free to contact with me , thank you!

Dioxaborolane Series is widely used in Suzuki reaction

The Suzuki reaction is an organic reaction, classified as a coupling reaction, where the coupling partners are a boronic acid and an organohalide catalyzed by a palladium(0) complex. It was first published in 1979 by Akira Suzuki and he shared the 2010 Nobel Prize in Chemistry with Richard F. Heck and Ei-ichi Negishi for their effort for discovery and development of palladium-catalyzed cross couplings in organic synthesis. In many publications this reaction also goes by the name Suzuki–Miyaura reaction and is also referred to as the Suzuki coupling. It is widely used to synthesize poly-olefins, styrenes, and substituted biphenyls. Several reviews have been published describing advancements and the development of the Suzuki Reaction.[5][6][7] The general scheme for the Suzuki reaction is shown below where a carbon-carbon single bond is formed by coupling an organoboron species (R1-BY2) with a halide (R2-X) using a palladium catalyst and a base.




Dioxaborolane Series

Dioxaborolane Series,214360-69-7 Large Scale,214360-69-7 In Stock,1356963-11-5 Large Scale

Jinan Meigao Biopharmaceutical Technology Co., Ltd. , http://www.meigaobiopharma.com

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