2,3-Dichloro-1-propene TCI D0406

Chemical Identity

Other names: 2-Chloroallyl Chloride
CAS No.: 78-88-6
PubChem: CID 6565·SID 87567088
Formula: C3H4Cl2
Molecular weight: 110.97 g/mol
Purity: >97.0%(GC)
Storage: 0-10°C
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2,3-dichloroprop-1-ene
SMILES: C=C(CCl)Cl
InChIKey: FALCMQXTWHPRIH-UHFFFAOYSA-N
MDL: MDL00000943

Rp 1.008.000,00

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2,3-Dichloro-1-propene is a chemical compound widely used in organic synthesis to create complex organic molecules. It serves as a key building block in various chemical reactions, particularly in the development of longer carbon chains. Its simple molecular structure plays a crucial role in enabling the formation of more intricate chemical structures. In the laboratory, this compound is essential for both substitution and addition reactions, making it a versatile reagent in synthetic chemistry. Its utility extends to the synthesis of aromatic and heterocyclic compounds, where its reactivity and structural characteristics are highly valued.

The compound's chemical properties make it a preferred choice for controlled synthetic processes. It exhibits stability under specific conditions but remains reactive to environmental factors such as high temperature and humidity. This reactivity allows it to participate in a wide range of chemical transformations. The presence of chlorine atoms on two carbon positions imparts polarity, which influences its interactions with solvents and other reagents. These characteristics make it ideal for applications requiring precise control over reactivity and chemical behavior.

In Indonesian laboratories, 2,3-Dichloro-1-propene is commonly used in organic chemistry research, particularly in academic and research institutions. Its availability and chemical properties make it an essential component of chemical supplies in local laboratories. Researchers rely on this compound for its role in synthesizing complex organic compounds, supporting both educational and scientific advancements in the field.

Related TCI products

Organic synthesis is a key application where 2,3-Dichloro-1-propene is used to build complex molecular structures through substitution and addition reactions.
Aromatic compound synthesis benefits from its reactivity and ability to form stable intermediates in the creation of aromatic rings.
Heterocyclic compound synthesis relies on its structural versatility and reactivity for forming ring systems with diverse functionalities.
Teaching laboratories use it to demonstrate chemical reactivity and synthetic techniques in undergraduate and graduate courses.
Research institutions incorporate it into studies focused on chemical reactivity, reaction mechanisms, and synthetic pathways.

Brand	TCI
CAS number	78-88-6
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Liquid
Storage	Store in a cool, dry place away from light and incompatible materials

This compound should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of materials compatible with its chemical properties, such as glass or high-density polyethylene. Due to its reactivity, it should be kept away from incompatible substances like strong oxidizing agents or moisture. In laboratory settings, proper ventilation and personal protective equipment should be used when handling. Regular monitoring of storage conditions is essential to maintain its stability and ensure safe handling. Always follow standard chemical safety protocols to minimize risks associated with its use and storage.

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