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Benzene, 1-ethyl-4-pentyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34350-07-7

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34350-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34350-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,3,5 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 34350-07:
(7*3)+(6*4)+(5*3)+(4*5)+(3*0)+(2*0)+(1*7)=87
87 % 10 = 7
So 34350-07-7 is a valid CAS Registry Number.

34350-07-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name p-ethylamylbenzene

1.2 Other means of identification

Product number -
Other names 1-Ethyl-4-n-amylbenzol

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:34350-07-7 SDS

34350-07-7Relevant academic research and scientific papers

Nickel-Catalyzed Stereodivergent Synthesis of E- and Z-Alkenes by Hydrogenation of Alkynes

Murugesan, Kathiravan,Bheeter, Charles Beromeo,Linnebank, Pim R.,Spannenberg, Anke,Reek, Joost N. H.,Jagadeesh, Rajenahally V.,Beller, Matthias

, p. 3363 - 3369 (2019)

A convenient protocol for stereodivergent hydrogenation of alkynes to E- and Z-alkenes by using nickel catalysts was developed. Simple Ni(NO3)2?6 H2O as a catalyst precursor formed active nanoparticles, which were effective for the semihydrogenation of several alkynes with high selectivity for the Z-alkene (Z/E>99:1). Upon addition of specific multidentate ligands (triphos, tetraphos), the resulting molecular catalysts were highly selective for the E-alkene products (E/Z>99:1). Mechanistic studies revealed that the Z-alkene-selective catalyst was heterogeneous whereas the E-alkene-selective catalyst was homogeneous. In the latter case, the alkyne was first hydrogenated to a Z-alkene, which was subsequently isomerized to the E-alkene. This proposal was supported by density functional theory calculations. This synthetic methodology was shown to be generally applicable in >40 examples and scalable to multigram-scale experiments.

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