(S)-2,4-Dichloro-alpha-(chloromethyl)benzyl Alcohol TCI D5115

Chemical Identity

Other names: (S)-2-Chloro-1-(2,4-dichlorophenyl)ethanol
CAS No.: 126534-31-4
PubChem: CID 5324672·SID 468591291
Formula: C8H7Cl3O
Molecular weight: 225.49 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (1S)-2-chloro-1-(2,4-dichlorophenyl)ethanol
SMILES: C1=CC(=C(C=C1Cl)Cl)C(CCl)O
InChIKey: XHEPANNURIQWRM-MRVPVSSYSA-N
MDL: MDL07776655

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(S)-2,4-Dichloro-alpha-(chloromethyl)benzyl Alcohol is a chiral building block widely used in asymmetric synthesis to construct complex molecular structures. This compound plays a crucial role in the development of bioactive molecules by enabling the creation of stereoisomers with specific spatial arrangements. Its chiral nature makes it an essential tool in laboratories aiming to achieve precise control over stereochemistry during synthetic processes. As a key component in the field of asymmetric synthesis, it supports the design of pharmaceuticals and organic compounds with desired biological activities.

The compound's unique chemical properties, including its ability to form stable intermediates under controlled conditions, make it a preferred choice for researchers. Its reactivity allows it to participate in various synthetic transformations, contributing to the formation of target molecules with high stereochemical fidelity. The stability of the compound under specific conditions further enhances its reliability in laboratory settings, ensuring consistent results in experimental procedures. These characteristics make it a versatile and dependable material for advanced chemical research.

In Indonesian laboratories, this compound is commonly used in organic chemistry, pharmacology, and biochemical research. It is particularly valuable for studies requiring precise stereoselective synthesis, such as the development of new drugs or functional materials. Researchers in academic and industrial settings often rely on this compound to achieve the desired stereochemistry in their experiments, making it an essential reagent in the chemical research landscape of Indonesia.

TCI brochures (PDF)

Chiral Building Blocks 2025-04-14 · p. 9

Related TCI products

Organic chemistry research utilizes this compound for the synthesis of chiral molecules with specific stereochemical configurations.
Pharmacological studies benefit from its ability to generate stereoisomers, aiding in the development of bioactive pharmaceuticals.
Biochemical experiments leverage its chiral properties to study enzyme interactions and molecular recognition processes.
Asymmetric synthesis projects rely on its structural features to create complex molecules with controlled stereochemistry.
Industrial chemical processes incorporate it for the production of specialty chemicals requiring precise stereochemical control.

Brand	TCI
CAS number	126534-31-4
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Liquid or solid, depending on the specific product variant
Storage	Store in a cool, dry place away from light and incompatible materials

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a tightly sealed container to prevent moisture absorption and contamination. Due to its chemical nature, it should be stored separately from strong oxidizing agents or reactive substances to avoid potential chemical interactions. In laboratory settings, proper personal protective equipment, such as gloves and safety goggles, should be worn when handling the compound. Regular monitoring of storage conditions is essential to maintain its stability and ensure safe usage in research applications.

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