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2-Pyrrolidinone, 1-(1,3-butadienyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112682-86-7

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112682-86-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112682-86-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,6,8 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112682-86:
(8*1)+(7*1)+(6*2)+(5*6)+(4*8)+(3*2)+(2*8)+(1*6)=117
117 % 10 = 7
So 112682-86-7 is a valid CAS Registry Number.

112682-86-7SDS

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 (1'E)-N-(buta-1',3'-dienyl)pyrrolidin-2-one

1.2 Other means of identification

Product number -
Other names ((E)-1-Buta-1,3-dienyl)-pyrrolidin-2-one

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:112682-86-7 SDS

112682-86-7Upstream product

112682-86-7Relevant academic research and scientific papers

Bi-directional alkyne tandem isomerization via Pd(0)/carboxylic acid joint catalysis: expedient access to 1,3-dienes

Cera, Gianpiero,Lanzi, Matteo,Bigi, Franca,Maggi, Raimondo,Malacria, Max,Maestri, Giovanni

supporting information, p. 14021 - 14024 (2019/01/03)

An in situ formed palladium hydride catalyst enables the sequential dual isomerization of propargylamide derivatives to 1-amido-1,3-dienes with high chemo- and regioselectivity. The reaction shows ample functional group tolerance, delivering a valuable class of products, including highly deuterated ones, from readily available reagents. The reaction occurs through a complex mechanism studied by DFT modelling.

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