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1-Chloro-3-ethoxypropane, also known as ethyl chloropropyl ether, is an organic chemical compound characterized by its molecular formula C5H11ClO. It is a clear, colorless liquid with a distinctive odor, and its molecular structure features a chlorine atom and an ethoxy group. This combination endows 1-Chloro-3-ethoxypropane with a wide range of applications in chemical synthesis and as an intermediate in the production of various organic compounds, including pharmaceuticals and pesticides.

36865-38-0

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36865-38-0 Usage

Uses

Used in Pharmaceutical Industry:
1-Chloro-3-ethoxypropane is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows for versatile reactions that can lead to the creation of a range of medicinal agents.
Used in Pesticide Production:
In the agricultural sector, 1-Chloro-3-ethoxypropane serves as an intermediate in the production of pesticides. Its reactivity and ability to form stable compounds make it a valuable component in developing effective pest control agents.
Used as a Solvent in Organic Synthesis:
1-Chloro-3-ethoxypropane is utilized as a solvent in various organic synthesis processes. Its properties as a clear, colorless liquid with a characteristic odor make it suitable for dissolving a range of substances in chemical reactions.
Used as a Reagent in Organic Chemistry:
Due to its reactive nature, 1-Chloro-3-ethoxypropane is employed as a reagent in organic chemistry. It can participate in numerous chemical reactions, facilitating the formation of desired products in the synthesis of complex organic compounds.
Safety Considerations:
It is crucial to handle 1-Chloro-3-ethoxypropane with care due to its flammable nature and potential to cause skin and respiratory irritation upon prolonged exposure. Proper safety measures should be implemented during its use to ensure the well-being of individuals and the integrity of the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 36865-38-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,6 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 36865-38:
(7*3)+(6*6)+(5*8)+(4*6)+(3*5)+(2*3)+(1*8)=150
150 % 10 = 0
So 36865-38-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H11ClO/c1-2-7-5-3-4-6/h2-5H2,1H3

36865-38-0SDS

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-Chloro-3-ethoxypropane

1.2 Other means of identification

Product number -
Other names 1-ethoxy-3-chloro-propane

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:36865-38-0 SDS

36865-38-0Relevant academic research and scientific papers

Dibenzo[bd]pyran derivatives, process for the preparation thereof and pharmaceutical compositions containing same

-

, (2008/06/13)

2,6-di-O-methyl-beta-cyclodextrin complexes of compounds of the formula (1a) STR1 wherein R2' stands for C1 to C12 alkyl or a group of the formula STR2 in which R11 is C1 to C4 alkyl; R12 is hydrogen or C1 to C4 alkyl; n is 0 or 1; p is 1 to 4; r is 1 to 4; and R3' and R4' are each C1 to C4 alkyl, or pharmaceutically salts thereof are disclosed, having analgesic activity.

SYNTHESIS OF Li + -SELECTIVE POLYETHER CARRIERS AND THEIR BEHAVIOR IN CATION TRANSPORT THROUGH LIQUID MEMBRANES.

Hiratani,Taguchi,Sugihara,Iio

, p. 1976 - 1984 (2007/10/02)

Noncyclic polyethers exhibiting lithium ion selectivity have been synthesized. Their competitive alkali-metal-ion transport through liquid membranes has been investigated, and the influence of their structures on the rates and selectivities of cation tran

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