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1-Ethyl-1-methylcyclopentane is a cycloalkane chemical compound with the molecular formula C9H18. It is a derivative of 1-methylcyclopentane, featuring an ethyl group attached to the methyl group. As a hydrocarbon, it exists as a colorless liquid with a slightly sweet odor. 1-ETHYL-1-METHYLCYCLOPENTANE is utilized in the production of other chemicals and serves as a solvent in various industrial processes. It exhibits low acute toxicity and is not considered to have a significant environmental impact. However, exposure to high concentrations may lead to irritation of the eyes, skin, and respiratory system, and there may be potential reproductive and developmental effects that require further research to understand fully.

16747-50-5

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16747-50-5 Usage

Uses

Used in Chemical Production:
1-Ethyl-1-methylcyclopentane is used as an intermediate in the synthesis of other chemicals for various applications due to its unique molecular structure and reactivity.
Used as a Solvent in Industrial Processes:
1-Ethyl-1-methylcyclopentane is used as a solvent in various industrial processes, taking advantage of its ability to dissolve a wide range of substances and its relatively low toxicity compared to other solvents.
Used in Research and Development:
Due to its unique properties, 1-ethyl-1-methylcyclopentane may be utilized in research and development settings to explore new chemical reactions, material formulations, or as a model compound for studying cycloalkane behavior.

Check Digit Verification of cas no

The CAS Registry Mumber 16747-50-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,4 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16747-50:
(7*1)+(6*6)+(5*7)+(4*4)+(3*7)+(2*5)+(1*0)=125
125 % 10 = 5
So 16747-50-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H16/c1-3-8(2)6-4-5-7-8/h3-7H2,1-2H3

16747-50-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ETHYL-1-METHYLCYCLOPENTANE

1.2 Other means of identification

Product number -
Other names 1-Ethyl-1-methylcyclopentan

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:16747-50-5 SDS

16747-50-5Relevant academic research and scientific papers

Unusual, CO Assisted Cyclo-oligomerization Reactions of Ethylene: Formation of Cyclopentane and Cyclohexane Derivatives by Ytterbium Ziegler-Natta Catalysts

Keim, Wilhelm,Chen, Zhongxin,Shen, Zhiquan

, p. 1923 - 1924 (1989)

A new oligomerization of ethene to alkylcyclopentanes and/or alkylcyclohexanes using YbCl3/AlEtCl2 or ZrCl4/AlEtCl2 Ziegler-Natta type catalysts is described in which addition of carbon monoxide is essential.

Energy Well of Diradicals, VII. - Conjugative-Stabilized Trimethylenemethane Derivatives. Geometry Dependance of the Singlet-Triplet Splitting

Roth, Wolfgang R.,Winzer, Markus,Korell, Michael,Wildt, Holger

, p. 897 - 920 (2007/10/02)

For the three 2,1'-bis-allyl diradicals 3-5 the singlet-triplet splitting has been determined by the oxygen-trapping technique.In agreement with theory the value for the planar diradical is large (>14 kcal*mol-1) whereas for the orthogonal geometry the energy gap is small (6.3 kcal*mol-1).In all cases a triplet groundstate is observed.From the rotational barrier of the exo methylene groups in 6 it is shown that the interconversion of the planar and orthogonal singlet states have activation barriers (6-9 kcal mol-1) which are responsible for their kinetic stability.In contrast to 6, where the formation of the orthogonal diradical proceeds by way of the planar diradical 3, the formation of the analogous orthogonal diradical 29 from homofulvene 17 is a concerted process.This difference is an important observation with respect to the fundamental understanding of concerted and non-concerted reactions. - Key Words: Diradicals / Gas-phase kinetics / Oxygen trapping / Dynamic gas chromatography / Rotational barrier, two-step

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