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5-ETHYLBICYCLO(2.2.1)-2-HEPTENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15403-89-1

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15403-89-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15403-89-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,0 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15403-89:
(7*1)+(6*5)+(5*4)+(4*0)+(3*3)+(2*8)+(1*9)=91
91 % 10 = 1
So 15403-89-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H14/c1-2-8-5-7-3-4-9(8)6-7/h3-4,7-9H,2,5-6H2,1H3

15403-89-1SDS

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 5-ETHYLBICYCLO(2.2.1)-2-HEPTENE

1.2 Other means of identification

Product number -
Other names 5-ethylnorbornene

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:15403-89-1 SDS

15403-89-1Upstream product

15403-89-1Relevant academic research and scientific papers

Stereoselectivity in a series of 7-alkylbicyclo[3.2.0]hept-2-enes: Experimental and computational perspectives

Leber, Phyllis,Kidder, Katherine,Viray, Don,Dietrich-Peterson, Eric,Fang, Yuan,Davis, Alexander

, (2018/08/03)

Rate constants for overall decomposition (kd) for a series of exo-7-alkylbicyclo[3.2.0]hept-2-enes are relatively invariant. For the alkyl substituents ethyl, propyl, butyl, isopropyl, and t-butyl, the ratio of the rate constant for [1,3] sigmatropic rearrangement to the rate constant for fragmentation, k13/kf, is significantly lower than k13/kf?=?150 observed for exo-7-methylbicyclo[3.2.0]hept-2-ene. Regardless of the size and mass of the alkyl group, the stereoselectivity of the [1,3] carbon migration appears to be quite stable at 80% to 89% suprafacial inversion (si), an observation consistent with conservation of angular momentum but not conservation of orbital symmetry. This global result comports with the phenomenon of “dynamic matching” espoused by Carpenter and collaborators for [1,3] sigmatropic rearrangements in general.

Oxygen-Deficient Tungsten Oxide as Versatile and Efficient Hydrogenation Catalyst

Song, Jiajia,Huang, Zhen-Feng,Pan, Lun,Zou, Ji-Jun,Zhang, Xiangwen,Wang, Li

, p. 6594 - 6599 (2015/11/18)

Heterogeneous hydrogenation is one of the most important industrial operations, and reduced metals (mostly noble metals and a few inexpensive metals) generally serve as the catalyst to activate molecular H2. Herein we report oxygen-deficient tungsten oxide, such as WO2.72, is a versatile and efficient catalyst for the hydrogenation of linear olefins, cyclic olefins, and aryl nitro groups, with obvious advantages compared with non-noble metal nickel catalyst from the aspect of activity and selectivity. Density functional theory calculations prove the oxygen-deficient surface activates H2 very easily in both kinetics and thermodynamics. Testing on several oxygen-deficient tungsten oxides shows a linear dependence between the hydrogenation activity and oxygen vacancy concentration. Tungsten is earth-abundant, and WO2.72 can be synthesized in large scale using a low-cost procedure, which provides an ideal catalyst for industrial application. Because oxygen vacancy is a common characteristic of many metal oxides, the findings in this work may be extended to other metal oxides and thus provide the possibility for exploring a new type of hydrogenation catalyst.

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