1191-95-3 Cyclobutanone

1191-95-3 Cyclobutanone Introduction

We are a pharmaceutical intermediate manufacturer of Cyclobutanone.

Its CAS No. is 1191-95-3.

Cyclobutanone is an organic compound that belongs to the class of ketones. Its chemical structure features a four-membered ring (cyclobutane) with a carbonyl group (C=O) attached to one of the carbons in the ring. The chemical formula of cyclobutanone is C4H6O.

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

1191-95-3 Cyclobutanone Specifications

1191-95-3 Cyclobutanone PDF

1191-95-3 CYCLOBUTANONE.pdf

1191-95-3 Cyclobutanone Factory display

Office Environment

Laboratory

Workshop/Warehouse

1191-95-3 Cyclobutanone Certification

Certificate

1191-95-3 Cyclobutanone FAQ

1. Manufacturer or trading company for 1191-95-3 Cyclobutanone?

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

2. 1191-95-3 Cyclobutanone 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 1191-95-3 Cyclobutanone?

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

4. What the MOQ of 1191-95-3 Cyclobutanone?

Please contact our sales team for more details.

5. What is 1191-95-3 Cyclobutanone?

Cyclobutanone is an organic compound consisting of a cyclobutane ring (a four-membered carbon ring) with a carbonyl group (C=O) attached to one of the carbons in the ring. It has the chemical formula C4H6O and is categorized as a ketone.

6. What are the key features of 1191-95-3 Cyclobutanone?

· Cyclobutane Ring: Cyclobutanone has a strained four-membered ring, which can contribute to reactivity in chemical reactions.

· Carbonyl Group: The carbonyl group (C=O) is attached to one of the carbons in the cyclobutane ring. This functional group imparts polarity and makes cyclobutanone reactive in nucleophilic addition reactions.

7. How is 1191-95-3 Cyclobutanone synthesized?

Cyclobutanone is typically synthesized via several methods:

· Cyclization of β-keto esters: One common approach involves the intramolecular cyclization of β-keto esters, where a reactive intermediate undergoes ring closure.

· Photochemical or thermal methods: Cyclobutanone can also be synthesized under specific conditions, such as photochemical or thermal decomposition of precursors like cyclobutyl hydroperoxide.

8. What are the uses of 1191-95-3 Cyclobutanone?

Cyclobutanone is primarily used as an intermediate in organic synthesis. It can be involved in the creation of more complex organic molecules, including those used in:

· Pharmaceuticals: Cyclobutanone is sometimes used as a starting material for the synthesis of bioactive molecules.

· Polymer Chemistry: It can be used in the preparation of polymers and other functionalized organic materials.

· Chemical Reactions: Due to the strained nature of its ring, cyclobutanone is useful in ring-opening reactions and other synthetic transformations in organic chemistry.

9. What are the physical properties of 1191-95-3 Cyclobutanone?

· Appearance: Cyclobutanone is typically a colorless liquid at room temperature.

· Boiling Point: It has a boiling point around 79°C.

· Melting Point: The melting point of cyclobutanone is about 48°C.

· Solubility: It is soluble in most organic solvents (like ether, chloroform, and acetone) but is sparingly soluble in water.

10. Is 1191-95-3 Cyclobutanone toxic?

Cyclobutanone is a relatively low-toxicity compound, but as with any chemical, it should be handled with care. It can cause irritation to the skin, eyes, and respiratory system if inhaled or in contact with skin. Proper personal protective equipment (PPE), including gloves and goggles, should be worn when handling it, and it should be used in well-ventilated areas.

11. How does the structure of 1191-95-3 Cyclobutanone influence its reactivity?

The four-membered cyclobutane ring creates ring strain, which makes the molecule more reactive than a non-cyclic ketone. This strain facilitates nucleophilic attack on the carbonyl group and promotes various organic reactions, such as ring-opening reactions and other electrophilic substitution processes.

12. What are the potential hazards associated with 1191-95-3 Cyclobutanone?

· Flammability: Like many organic solvents, cyclobutanone is flammable, and precautions should be taken to avoid open flames or sparks in areas where it is used.

· Health Hazards: Prolonged or repeated exposure may cause irritation, and inhaling the vapors can be harmful. Inhalation, skin contact, or ingestion should be avoided.

13. What is the stability of 1191-95-3 Cyclobutanone?

Cyclobutanone is relatively stable under normal conditions. However, due to the strained ring structure, it can undergo ring-opening reactions under certain conditions, especially when exposed to nucleophiles or other reactive species. It should be stored in airtight containers to protect it from moisture and air.

14. Can 1191-95-3 Cyclobutanone undergo reactions with nucleophiles?

Yes, cyclobutanone can undergo nucleophilic addition reactions at the carbonyl group, as the strained ring increases the electrophilicity of the carbonyl carbon. This reactivity is commonly utilized in synthetic organic chemistry for constructing more complex molecules.