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112426-02-5

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112426-02-5 Usage

Uses

Different sources of media describe the Uses of 112426-02-5 differently. You can refer to the following data:
1. LITHIUM 2-THIENYLCYANOCUPRATE 0.25M is useful reagent for the preparation of higher-order cuprates.1
2. Useful reagent for the preparation of higher-order cuprates.

General Description

Learn More at the Professor and Product Portal of Professor Bruce Lipshutz.

Check Digit Verification of cas no

The CAS Registry Mumber 112426-02-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,4,2 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 112426-02:
(8*1)+(7*1)+(6*2)+(5*4)+(4*2)+(3*6)+(2*0)+(1*2)=75
75 % 10 = 5
So 112426-02-5 is a valid CAS Registry Number.

112426-02-5 Well-known Company Product Price

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  • Aldrich

  • (324175)  Lithium2-thienylcyanocupratesolution  0.25 M in THF

  • 112426-02-5

  • 324175-100ML

  • 532.35CNY

  • Detail
  • Aldrich

  • (324175)  Lithium2-thienylcyanocupratesolution  0.25 M in THF

  • 112426-02-5

  • 324175-800ML

  • 2,261.61CNY

  • Detail

112426-02-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name lithium,azanidylidenemethylidenecopper,2H-thiophen-2-ide

1.2 Other means of identification

Product number -
Other names 2-thienyl(cyano)copper lithium

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:112426-02-5 SDS

112426-02-5Relevant articles and documents

Effects of BF3*Et2O on Higher Order Organocuprate Reactions: Substrate Activation or Cuprate Modification?

Lipshutz, Bruce H.,Ellsworth, Edmund L.,Siahaan, Teruna J.

, p. 4834 - 4835 (1988)

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12-ARYL PROSTAGLANDIN ANALOGS

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Page/Page column 38-39; 48-49, (2010/11/08)

Compounds comprising the formula (I) are disclosed, wherein Y, A, X, R, D, and n are as described. A compound comprising a prostaglandin EP2 selective agonist wherein the ω-chain comprises a substituted phenyl, wherein at least one substituent

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