13250-82-3

  • Product Name:2-(3-Thienyl)-1,3-dioxolane
  • Molecular Formula:C7H8O2S
  • Purity:99%
  • Molecular Weight:156.205
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Product Details;

CasNo: 13250-82-3

Molecular Formula: C7H8O2S

factory and supplier 13250-82-3 2-(3-Thienyl)-1,3-dioxolane in stock

  • Molecular Formula:C7H8O2S
  • Molecular Weight:156.205
  • Vapor Pressure:0.0453mmHg at 25°C 
  • Refractive Index:1.553 
  • Boiling Point:245.3 °C at 760 mmHg 
  • Flash Point:102.2 °C 
  • PSA:46.70000 
  • Density:1.254 g/cm3 
  • LogP:1.79350 

3-Thiophenecarboxaldehyde ethylene acetal(Cas 13250-82-3) Usage

General Description

3-Thiophenecarboxaldehyde ethylene acetal is a chemical compound with the molecular formula C9H10O2S. It is a colorless to pale yellow liquid with a strong odor. 3-Thiophenecarboxaldehyde ethylene acetal is commonly used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and fragrances. It is also used as a flavoring agent in the food industry. 3-Thiophenecarboxaldehyde ethylene acetal is a versatile intermediate in organic synthesis, and its unique structure makes it an important precursor in the production of a wide range of valuable compounds. It is important to handle this chemical with caution as it may be harmful if ingested or inhaled, and can cause skin and eye irritation.

InChI:InChI=1/C7H8O2S/c1-4-10-5-6(1)7-8-2-3-9-7/h1,4-5,7H,2-3H2

13250-82-3 Relevant articles

Small isomeric push-pull chromophores based on thienothiophenes with tunable optical (non)linearities

Podlesny, Jan,Pytela, Old?ich,Klikar, Milan,Jelínková, Veronika,Kityk, Iwan V.,Ozga, Katarzyna,Jedryka, Jaroslaw,Rudysh, Myron,Bure?, Filip

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Method for preparing thiophene borate

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Paragraph 0012; 0014; 0019; 0021; 0026; 0028, (2018/09/21)

The invention relates to a method for pr...

HETEROARYL COMPOUNDS USEFUL AS INHIBITORS OF SUMO ACTIVATING ENZYME

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Paragraph 00332, (2016/01/25)

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13250-82-3 Process route

3-thiophene carboxaldehyde
498-62-4

3-thiophene carboxaldehyde

ethylene glycol
107-21-1

ethylene glycol

2-(thiophen-3-yl)-1,3-dioxolane
13250-82-3

2-(thiophen-3-yl)-1,3-dioxolane

Conditions
Conditions Yield
With toluene-4-sulfonic acid; In toluene; at 165 ℃; for 6h;
99%
With toluene-4-sulfonic acid; In benzene; Heating;
97%
toluene-4-sulfonic acid; In toluene; for 4h; Heating / reflux;
95.9%
With pyridinium p-toluenesulfonate; In benzene; for 6h; Dean-Stark; Reflux;
75%
With toluene-4-sulfonic acid; In toluene; at 120 ℃; for 8h; Temperature;
72%
With p-toluenesulfonic acid monohydrate; In benzene;
With toluene-4-sulfonic acid; In benzene; for 4h; Dean-Stark; Reflux;
With toluene-4-sulfonic acid; In toluene; for 24h; Reflux;
With pyridinium p-toluenesulfonate;
3-thiophene carboxaldehyde
498-62-4

3-thiophene carboxaldehyde

2-(thiophen-3-yl)-1,3-dioxolane
13250-82-3

2-(thiophen-3-yl)-1,3-dioxolane

Conditions
Conditions Yield
With p-toluenesulfonic acid monohydrate; In ethylene glycol; benzene;
91%
87%
With toluene-4-sulfonic acid; In benzene;
45.3 g (72%)
With pyridinium p-toluenesulfonate; In ethylene glycol; toluene;
12.1g (77.3 mmol, 86.7%)
With p-toluenesulfonic acid monohydrate; In ethylene glycol; toluene;

13250-82-3 Upstream products

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    498-62-4

    3-thiophene carboxaldehyde

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    107-21-1

    ethylene glycol

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    3-Bromomethylthiophene

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    3-Methylthiophene

13250-82-3 Downstream products

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    2-bromothiophene-3-carbaldehyde

  • 13250-83-4
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    2,3-Thiophenedicarbaldehyde 3-(Ethylene acetal)

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    3-(1,3-dioxolan-2-yl)thiophene-2-sulfonyl chloride

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