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1,1-dichloro-2-ethoxycyclopropane is a specific organic chemical compound that belongs to the family of organochlorine compounds, characterized by the presence of carbon-chlorine bonds. It features a cyclopropane ring, which is a triangular arrangement of three carbon atoms, with two chlorines attached to one carbon and an ethoxy group (an oxygen with an ethyl group attached) on a second carbon. This molecule is known for its potent chemical reactivity and is utilized in various organic chemical syntheses. Due to its reactivity and potential toxicity, it is crucial to handle 1,1-dichloro-2-ethoxycyclopropane with appropriate safety measures.

7363-99-7

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7363-99-7 Usage

Uses

Used in Organic Chemical Syntheses:
1,1-dichloro-2-ethoxycyclopropane is used as a key intermediate in the synthesis of various organic compounds. Its unique structure and reactivity make it a valuable building block for creating complex molecules in the fields of pharmaceuticals, agrochemicals, and materials science.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,1-dichloro-2-ethoxycyclopropane is used as a starting material for the synthesis of certain drugs. Its reactivity allows for the formation of new chemical bonds, which can lead to the development of novel therapeutic agents with improved efficacy and safety profiles.
Used in Agrochemical Industry:
1,1-dichloro-2-ethoxycyclopropane is employed as a precursor in the production of agrochemicals, such as pesticides and herbicides. Its chemical properties enable the creation of active ingredients that can effectively control pests and weeds, thereby contributing to increased crop yields and agricultural productivity.
Used in Materials Science:
In the field of materials science, 1,1-dichloro-2-ethoxycyclopropane is used as a component in the development of new materials with specific properties. Its incorporation into polymers and other materials can result in enhanced characteristics, such as improved strength, flexibility, or chemical resistance, which can be beneficial in various applications, including electronics, automotive, and aerospace industries.

Check Digit Verification of cas no

The CAS Registry Mumber 7363-99-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,6 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7363-99:
(6*7)+(5*3)+(4*6)+(3*3)+(2*9)+(1*9)=117
117 % 10 = 7
So 7363-99-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H8Cl2O/c1-2-8-4-3-5(4,6)7/h4H,2-3H2,1H3

7363-99-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dichloro-2-ethoxycyclopropane

1.2 Other means of identification

Product number -
Other names 1,1-dichloro-2-ethoxy-cyclopropane

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:7363-99-7 SDS

7363-99-7Relevant academic research and scientific papers

Multivariate optimization of a cyclopropanation, the key step in the synthesis of 3,3,4,4-tetraethoxybut-1-yne

Shang, Weidong,Terranova, Mariangela,Sydnes, Leiv K.,Bjorsvik, Hans-Rene

, p. 891 - 896 (2014)

3,3,4,4-Tetraethoxybut-1-yne (TEB) is a versatile synthon that can be produced in a four-step synthesis. The third step of the synthesis is a cycloproanation, which has been thoroughly investigated and optimized by means of statistical experimental design and multivariate modeling. At the outset, an exhaustively pre-experimental design was performed resulting in a copious Ishikawa cause-effect diagram. In total six of the experimental variables were assessed to be of large importance and thus selected for further investigation by fractional factorial design. The results of that screening and first step optimization formed the basis for a response surface modeling (RSM) study. The RSM investigation was completed by using a central composite design from which a response surface was graphically produced as an iso-contour projection. The derived multivariate predictive model in terms the iso-contour projection plots were ultimately utilized to establish experimental conditions that concomitantly provided excellent yield (>99%) and minimized amounts of inputs and thus obtain the desired product at the lowest production cost and minimized side-streams.

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