o-Chloranil TCI T0970

Chemical Identity

CAS No.: 2435-53-2
PubChem: CID 73252·SID 87576782
Formula: C6Cl4O2
Molecular weight: 245.9 g/mol
Purity: >97.0%(HPLC)(T)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3,4,5,6-tetrachlorocyclohexa-3,5-diene-1,2-dione
SMILES: C1(=C(C(=O)C(=O)C(=C1Cl)Cl)Cl)Cl
InChIKey: VRGCYEIGVVTZCC-UHFFFAOYSA-N

Rp 3.021.900,00

~~Rp 2.128.350,00~~ Rp 3.021.900,00

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Berat 5g 25g

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o-Chloranil is a chemical compound widely used in various organic reactions, particularly in the synthesis of heterocyclic and aromatic compounds. As a key building block in organic chemistry, it plays a crucial role in laboratory settings where complex molecular structures are being developed. Its unique molecular structure, featuring chlorine atoms at the ortho positions of aniline, contributes to its high reactivity and versatility in chemical transformations. This makes it an essential reagent for chemists working on a wide range of synthetic pathways.

The properties of o-Chloranil that make it a preferred choice include its ability to participate in electrophilic substitution and oxidation reactions. Its chemical stability under certain conditions, combined with its reactivity towards various reagents such as alkali metals, strong acids, and electrophilic compounds, enhances its utility in synthetic chemistry. These characteristics allow researchers to manipulate molecular structures with precision, making it a valuable tool in both academic and industrial research environments.

In Indonesian laboratories, o-Chloranil is a relevant material for organic chemistry research, particularly in higher education institutions and research centers. Its melting and boiling points enable its use across a range of experimental conditions, supporting diverse applications in chemical synthesis. Its reliability and flexibility make it a go-to compound for researchers aiming to explore new chemical reactions and molecular designs.

TCI brochures (PDF)

Ligands 2025-12-01 · p. 19

Related TCI products

Organic synthesis for the creation of heterocyclic and aromatic compounds due to its reactivity and structural versatility.
Electrophilic substitution reactions where its chlorine substituents facilitate selective chemical transformations.
Oxidation processes in which o-Chloranil acts as an oxidizing agent for various organic substrates.
Research in medicinal chemistry for the development of pharmaceutical compounds and bioactive molecules.
Teaching and experimental demonstrations in undergraduate and graduate chemistry courses for hands-on learning.

Brand	TCI
CAS number	2435-53-2
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid
Storage	Store in a cool, dry place away from moisture and direct sunlight

o-Chloranil should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in airtight containers to prevent exposure to moisture and air, which can affect its reactivity. Due to its high reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to avoid contact with strong acids, alkali metals, and other reactive substances to prevent unwanted chemical reactions. In laboratory settings, it should be stored separately from incompatible materials to ensure safety and maintain the integrity of the compound.

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