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3-Cyclobutene-1,2-dione, 3,4-dibutyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

122967-65-1

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122967-65-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122967-65-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,9,6 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 122967-65:
(8*1)+(7*2)+(6*2)+(5*9)+(4*6)+(3*7)+(2*6)+(1*5)=141
141 % 10 = 1
So 122967-65-1 is a valid CAS Registry Number.

122967-65-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-di-n-butyl-3-cyclobutene-1,2-dione

1.2 Other means of identification

Product number -
Other names .3,4-dibutylcyclobut-3-ene-1,2-dione

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:122967-65-1 SDS

122967-65-1Relevant academic research and scientific papers

Reactive iron carbonyl reagents via reaction of metal alkoxides with Fe(CO)5 or Fe2(CO)9: Synthesis of cyclobutenediones via double carbonylation of alkynes

Beesu, Mallesh,Periasamy, Mariappan

experimental part, p. 543 - 549 (2011/04/16)

Alkoxy bases such as t-BuOK react with Fe(CO)5 to give reactive iron carbonyl intermediates that in turn react with alkynes at 70 °C in THF to give 1,2-cyclobutenediones in 70-93% yields after CuCl2· 2H2O oxidation. A novel 1,2-diacyloxyferrole derivative was isolated in the reaction of diphenylacetylene with Fe(CO)5/t-BuOK in the presence of acetyl chloride in contrast to the formation of a 1,4-diacyloxyferrole complex formed in the reaction using Fe(CO) 5/Me3NO. The Fe2(CO)9/t-BuOK reagent system also converts the alkynes to corresponding cyclobutenediones in 63-90% yields under similar reaction conditions.

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