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1184-54-9

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1184-54-9 Usage

Uses

Copper(II) methoxide is used as primary and secondary intermediates. Treatment of these methoxide derivatives with excess water results in the clean formation of mononuclear copper(II) hydroxide complexes.

Check Digit Verification of cas no

The CAS Registry Mumber 1184-54-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,8 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1184-54:
(6*1)+(5*1)+(4*8)+(3*4)+(2*5)+(1*4)=69
69 % 10 = 9
So 1184-54-9 is a valid CAS Registry Number.

1184-54-9 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (18861)  Copper(II) methoxide, typically 98% (metals basis)   

  • 1184-54-9

  • 1g

  • 270.0CNY

  • Detail
  • Alfa Aesar

  • (18861)  Copper(II) methoxide, typically 98% (metals basis)   

  • 1184-54-9

  • 5g

  • 899.0CNY

  • Detail
  • Alfa Aesar

  • (18861)  Copper(II) methoxide, typically 98% (metals basis)   

  • 1184-54-9

  • 25g

  • 3735.0CNY

  • Detail

1184-54-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name copper,methanol

1.2 Other means of identification

Product number -
Other names cupric methoxide

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:1184-54-9 SDS

1184-54-9Relevant articles and documents

The Ullmann condensation reaction of haloanthraquinone derivatives with amines in aprotic solvents. VI. The combination of Cu(I) and hydroxo or alkoxo Cu(II) as effective catalyst system

Arai,Hashimoto,Yamagishi,Hida

, p. 3143 - 3149 (1989)

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Copper(II) oligomeric derivatives for deposition of copper thin films

Shahid, Muhammad,Tahir, Asif Ali,Hamid, Mazhar,Mazhar, Muhammad,Zeller, Matthias,Molloy, Kieran C.,Hunter, Allen D.

, p. 1043 - 1050 (2009)

Homobi-, -tri- and -tetranuclear copper(II) oligomeric complexes, [Cu(dmap)(OAc)(H2O)]2-H2O (1), [Cu 3(dmae)3(acac)2- Cl] (2) and [Cu(dmae)(TFA)]4 (3), have been prepared by reac

Copper(II) methoxide: Direct solventothermal synthesis and X-ray crystal structure

Nelson, Kendric J.,Guzei, Ilia A.,Lund, Gregory S.,McGaff, Robert W.

, p. 2017 - 2020 (2008/10/08)

Copper methoxide has been prepared under fairly mild solventothermal conditions by direct reaction of copper(II) acetate monohydrate and methanol. The product has been structurally characterized for the first time by single crystal X-ray diffraction and found to possess a novel infinite one-dimensional chain structure in which copper atoms in distorted square planar coordination environments are linked by bridging methoxide ligands. The conversion of copper acetate to copper methoxide is essentially quantitative. The major byproduct of the synthesis is methyl acetate.

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