Welcome to LookChem.com Sign In|Join Free
  • or
3-cyclobutene-1,2-dione is a chemical compound characterized by its molecular formula C4H4O2. It features a four-membered ring structure with two carbonyl groups, making it a cyclic diketone. 3-cyclobutene-1,2-dione is recognized for its reactivity and instability, which positions it as a significant intermediate in organic chemistry. Its molecular structure endows it with unique reactivity, allowing it to engage in various chemical reactions such as Diels-Alder cycloadditions, ene reactions, and nucleophilic additions. 3-cyclobutene-1,2-dione's utility as a building block for synthesizing complex organic molecules in the laboratory is further underscored by its ability to participate in these diverse reactions. Owing to its unstable nature, 3-cyclobutene-1,2-dione requires careful handling and storage to avert decomposition or unwanted chemical interactions.

32936-74-6

Post Buying Request

32936-74-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

32936-74-6 Usage

Uses

Used in Organic Synthesis:
3-cyclobutene-1,2-dione is utilized as a key reagent in organic synthesis for its ability to participate in a variety of chemical reactions. Its involvement in Diels-Alder cycloadditions, ene reactions, and nucleophilic additions makes it a valuable component in creating complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-cyclobutene-1,2-dione is employed as a building block for the synthesis of pharmaceutical compounds. Its reactivity and capacity to form stable intermediates in various chemical reactions contribute to the development of new drug molecules.
Used in Chemical Research:
3-cyclobutene-1,2-dione serves as a crucial intermediate in chemical research, particularly in the study of reaction mechanisms and the development of new synthetic methodologies. Its unique properties and reactivity provide researchers with opportunities to explore novel pathways and enhance existing synthetic processes.
Used in Material Science:
In material science, 3-cyclobutene-1,2-dione is used as a precursor in the synthesis of advanced materials with specific properties. Its role in creating complex molecular structures is vital for developing materials with tailored characteristics for various applications.
Used in Specialty Chemicals Production:
3-cyclobutene-1,2-dione is also used in the production of specialty chemicals, where its reactivity and instability are harnessed to create unique chemical entities that find use in niche applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 32936-74-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,9,3 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 32936-74:
(7*3)+(6*2)+(5*9)+(4*3)+(3*6)+(2*7)+(1*4)=126
126 % 10 = 6
So 32936-74-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H2O2/c5-3-1-2-4(3)6/h1-2H

32936-74-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclobut-3-ene-1,2-dione

1.2 Other means of identification

Product number -
Other names cyclobutene-1,2-dione

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:32936-74-6 SDS

32936-74-6Relevant academic research and scientific papers

CYCLOBUTENDION UND METHYLENCYCLOBUTENON. SYNTHESE, DIENOPHILE REAKTIVITAET UND EXO, ENDO-SELECTIVITAET

Martin, Hans-Dieter,Oftring, Alfred,Iden, Ruediger,Schwichtenberg, Evelyn,Schiwek, Hans-Joachim

, p. 841 - 844 (2007/10/02)

A new synthesis of cyclobutenedione and methylenecyclobutenone and their reactions with 1,3-dienes are described.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 32936-74-6