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Postion:Product Catalog >Organic Chemistry>Carboxylic acids and derivatives>Ethyl 1,4-benzodioxan-2-carboxylate(EBDC)
Ethyl 1,4-benzodioxan-2-carboxylate(EBDC)
  • Ethyl 1,4-benzodioxan-2-carboxylate(EBDC)
  • Ethyl 1,4-benzodioxan-2-carboxylate(EBDC)
  • Ethyl 1,4-benzodioxan-2-carboxylate(EBDC)
  • Ethyl 1,4-benzodioxan-2-carboxylate(EBDC)
  • Ethyl 1,4-benzodioxan-2-carboxylate(EBDC)

Ethyl 1,4-benzodioxan-2-carboxylate(EBDC) NEW

Price $600 $550 $500
Package 1kg 20kg 100kg
Min. Order: 1kg
Supply Ability: 100kgs/20days
Update Time: 2024-07-08
Related documents: NMR IR COA

Product Details

Product Name: Ethyl 1,4-benzodioxan-2-carboxylate(EBDC) CAS No.: 4739-94-0
Min. Order: 1kg Purity: 99%
Supply Ability: 100kgs/20days Release date: 2024/07/08

Ethyl 1,4-benzodioxan-2-carboxylate (EBDC) is a chemical compound that can be described by its systematic name and structural formula. It is an ester derivative of 1,4-benzodioxan-2-carboxylic acid, featuring an ethyl group attached to the carboxylate functionality.

Chemical Information

  • IUPAC Name: Ethyl 2,3-dihydro-1,4-benzodioxine-2-carboxylate

  • CAS Number: Not readily available

Structure and Properties

  • Molecular Formula: C11H12O4

  • Molecular Weight: Approximately 208.21 g/mol

  • Functional Groups:

    • Ester Group: Responsible for its reactivity in esterification and hydrolysis reactions.

    • Benzodioxan Ring: A fused bicyclic structure containing an oxygen-bridged aromatic ring.

Applications

EBDC may be used in organic synthesis, possibly as an intermediate for pharmaceuticals, agrochemicals, or other organic compounds due to its ester functionality which can be transformed into various other chemical groups.

Safety and Handling

As with many organic compounds, proper safety protocols should be followed. This includes using personal protective equipment (PPE) like gloves and goggles, working in a well-ventilated area, and understanding its Material Safety Data Sheet (MSDS) for detailed handling and disposal guidelines.

Synthesis

The synthesis of EBDC typically involves the esterification of 1,4-benzodioxan-2-carboxylic acid with ethanol, often using a dehydrating agent like sulfuric acid or a catalyst like p-toluenesulfonic acid (PTSA).

Further Reading

For more detailed information, refer to organic chemistry literature or specific research articles related to the synthesis and applications of benzodioxane derivatives. Online chemical databases and scientific journals can provide in-depth data on EBDC and its derivatives. Websites like PubChem, ChemSpider, and Google Scholar can be useful resources for finding such information.


Company Profile Introduction

SACH BIOTECH Co.,Ltd. was reorganized and established in 2023, formerly known as Hangzhou Shitai Biotech Co.,Ltd. The main body of the company is located by the beautiful West Lake of Hangzhou. The main production base is located in Shandong Province, China, and the pilot production base and laboratory are located in Henan province. After 15 years of hard work and accumulation, we now have a strong research and development team and experimental equipment, and the pilot plant can meet the requirements of different customers. The production base located in Shandong, China can meet the needs of customers for industrial scale production.

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