(R)-(+)-4-Chloro-3-hydroxybutyronitrile TCI C2763

Chemical Identity

CAS No.: 84367-31-7
Formula: C4H6ClNO
Molecular weight: 119.55 g/mol
Purity: >96.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (3R)-4-chloro-3-hydroxybutanenitrile
SMILES: C(C#N)C(CCl)O
InChIKey: LHBPNZDUNCZWFL-SCSAIBSYSA-N
MDL: MDL00273362
PubChem: CID 641056

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(R)-(+)-4-Chloro-3-hydroxybutyronitrile is a chiral compound widely used in asymmetric synthesis to create bioactive molecules. This chemical plays a crucial role in organic chemistry laboratories, particularly in the development of pharmaceuticals and specialty chemicals. Its chiral nature allows for precise control over stereochemistry, making it an essential tool for researchers aiming to synthesize complex molecules with specific spatial arrangements. Due to its optical activity, it is often employed in enantioselective reactions where the stereochemistry of the final product is critical.

The compound’s stability and controlled reactivity make it a preferred choice for synthetic chemists. Its ability to participate in various reaction conditions without significant degradation ensures reliable results in experimental setups. Additionally, its availability in high purity and consistent quality supports reproducibility in research. These properties make it a reliable and versatile reagent for advanced chemical synthesis.

In Indonesian laboratories, this compound is commonly used in pharmaceutical, organic chemistry, and biochemical research. It supports the development of new therapeutic agents and functional materials. Its presence in research institutions and academic settings highlights its importance in advancing scientific knowledge and innovation. The compound’s availability ensures that researchers can meet the demands of their experiments with precision and efficiency.

Asymmetric synthesis in pharmaceutical research for the creation of chiral compounds with specific biological activities.
Organic chemistry experiments requiring precise control over stereochemistry in complex molecule synthesis.
Biochemical studies involving the development of enzyme inhibitors and receptor ligands with defined spatial configurations.
Chiral building block applications in the design of new drugs and functional materials with tailored properties.
Research in medicinal chemistry for the synthesis of compounds with potential therapeutic applications in various disease models.

Brand	TCI
CAS number	84367-31-7
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in various quantities as per standard chemical supply specifications
Physical form	Liquid
Storage	Store in a cool, dry place away from light and incompatible substances

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of materials compatible with its chemical properties to prevent contamination and degradation. Due to its reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid exposure to incompatible substances, and always follow standard chemical handling procedures to maintain the integrity of the compound. Proper storage and handling are essential to ensure the compound remains effective and safe for use in research applications.

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