3721-95-7 Cyclobutanecarboxylic acid

3721-95-7 Cyclobutanecarboxylic acid Introduction

We are a pharmaceutical intermediate manufacturer of Cyclobutanecarboxylic acid.

Its CAS No. is 3721-95-7.

Cyclobutanecarboxylic acid is an organic compound with the chemical formula C5H8O2. It is a cyclic carboxylic acid that consists of a cyclobutane ring (a four-membered carbon ring) with a carboxyl group (-COOH) attached to one of the carbon atoms in the ring. The structure of the molecule gives it distinctive properties related to both the ring strain in the cyclobutane and the reactivity of the carboxyl group.

Our pharmaceutical intermediates can be used in a variety of APIs such as Articaine, Pyrantel, Bicalutamide, Apalutamide, etc.

3721-95-7 Cyclobutanecarboxylic acid Specifications

3721-95-7 Cyclobutanecarboxylic acid PDF

3721-95-7 CYCLOBUTANECARBOXYLIC ACID.pdf

3721-95-7 Cyclobutanecarboxylic acid Factory display

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3721-95-7 Cyclobutanecarboxylic acid Certification

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3721-95-7 Cyclobutanecarboxylic acid FAQ

1. Manufacturer or trading company for 3721-95-7 Cyclobutanecarboxylic acid?

Cyclobutanecarboxylic acid is produced by EASTFINE , and we are in charge of  overseas selling . Not just trading company .

2. 3721-95-7 Cyclobutanecarboxylic acid supplier and factories or wholesale locates in such countries like?

China,America,Brazil,England,Russia,Poland,India,Pakistan,NewZealand,Korea,Australia,Dubai,Turkey,Indonesia,UAE.

3. Can I get a sample for trying 3721-95-7 Cyclobutanecarboxylic acid?

Yes , you can have Cyclobutanecarboxylic acid sample for starting the business , but it is not free

4. What the MOQ of 3721-95-7 Cyclobutanecarboxylic acid?

Please contact our sales team for more details.

5. What is 3721-95-7 Cyclobutanecarboxylic acid?

Cyclobutanecarboxylic acid is an organic compound with the molecular formula C5H8O2. It consists of a cyclobutane ring (a four-membered carbon ring) attached to a carboxyl group (-COOH). This compound is part of the class of cyclic carboxylic acids and exhibits the typical reactivity of both strained cyclic compounds and carboxylic acids.

6. What are the uses of 3721-95-7 Cyclobutanecarboxylic acid?

· Organic Synthesis: Cyclobutanecarboxylic acid serves as an intermediate in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and polymers.

· Building Block for Chemical Reactions: It can undergo reactions such as esterification, decarboxylation, and ring-opening reactions due to the strain in the cyclobutane ring.

· Research: It is used in research settings to study strained ring systems and carboxylate chemistry.

7. How is 3721-95-7 Cyclobutanecarboxylic acid synthesized?

Cyclobutanecarboxylic acid can be synthesized using several methods, such as:

· Ring-closure reactions: Cyclobutane rings can be formed from precursor compounds that include a carboxyl group. One possible synthetic route involves starting with a linear carboxylic acid and employing cyclization techniques.

· Electrophilic addition reactions: The carboxyl group can be introduced onto a cyclobutane precursor using electrophilic substitution methods.

Specific synthetic pathways often depend on the desired substitution patterns and functional group compatibility.

8. What are the physical properties of 3721-95-7 Cyclobutanecarboxylic acid?

· Appearance: It is typically a white solid or crystalline substance.

· Boiling Point: Cyclobutanecarboxylic acid has a boiling point of around 210-215°C (410-419°F).

· Solubility: It is soluble in organic solvents like ethanol, acetone, and ether, but is poorly soluble in water due to the hydrophobic nature of the cyclobutane ring and the carboxyl group.

9. What reactions can 3721-95-7 Cyclobutanecarboxylic acid undergo?

· Esterification: Cyclobutanecarboxylic acid can react with alcohols to form esters, which are widely used in flavor, fragrance, and industrial applications.

· Decarboxylation: The carboxyl group can be removed by heating or in the presence of a decarboxylation agent to form a cyclobutane derivative.

· Ring-opening reactions: The strained cyclobutane ring can undergo ring-opening reactions, which can be useful for synthesizing other organic molecules or for studying ring strain.

· Reduction: It can be reduced to form a corresponding alcohol (cyclobutanemethanol) or other reduced products.

10. What is the significance of the cyclobutane ring in 3721-95-7 Cyclobutanecarboxylic acid?

The cyclobutane ring in cyclobutanecarboxylic acid introduces strain into the molecule, making it more reactive than non-cyclic carboxylic acids. This strain can be relieved through various chemical reactions, such as ring-opening reactions, which is useful in organic synthesis. The strain also impacts the compound's reactivity and the types of reactions it can undergo.

11. Is 3721-95-7 Cyclobutanecarboxylic acid toxic?

While cyclobutanecarboxylic acid is not highly toxic in small quantities, like many organic acids, it can cause irritation to the skin, eyes, and respiratory tract if proper safety precautions are not followed. Handling should be done with care, and appropriate personal protective equipment (PPE) such as gloves and goggles should be worn.

12. Can 3721-95-7 Cyclobutanecarboxylic acid be used in pharmaceuticals?

Yes, cyclobutanecarboxylic acid can serve as an intermediate in the synthesis of pharmaceutical compounds. The strained cyclobutane ring and the carboxyl group make it a useful building block for the development of bioactive molecules in medicinal chemistry.

13. How does the carboxyl group affect the reactivity of 3721-95-7 Cyclobutanecarboxylic acid?

The carboxyl group (-COOH) imparts typical carboxylic acid reactivity to the compound, enabling it to undergo reactions like esterification, reduction, and decarboxylation. Additionally, the presence of the carboxyl group can influence the compound’s solubility and acidity, making it a useful functional group in organic synthesis.