(R)-(+)-3-Benzyloxy-1,2-propanediol TCI B2141

Chemical Identity

CAS No.: 56552-80-8
PubChem: CID 2724795·SID 87565009
Formula: C10H14O3
Molecular weight: 182.22 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2R)-3-phenylmethoxypropane-1,2-diol
SMILES: C1=CC=C(C=C1)COC[C@@H](CO)O
InChIKey: LWCIBYRXSHRIAP-SNVBAGLBSA-N

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Berat 100mg 1g

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(R)-(+)-3-Benzyloxy-1,2-propanediol is a chiral building block widely used in asymmetric synthesis to construct molecules with specific biological activities. This compound plays a crucial role in organic chemistry laboratories, particularly in the development of optically active compounds. Its unique stereochemistry allows for precise control over the spatial arrangement of atoms, making it essential for creating complex molecular structures. As a key component in chiral synthesis, it supports the creation of enantiomerically pure compounds, which are vital in pharmaceutical and biomedical research.

The compound's chiral nature and optical activity make it a preferred choice for researchers aiming to achieve high selectivity in synthetic processes. Its ability to form distinct isomers enables the synthesis of compounds with specific stereochemical configurations, which are often required in drug development. Additionally, its chemical stability and compatibility with various reaction conditions contribute to its reliability in laboratory settings. These properties ensure consistent results and enhance the reproducibility of experiments, making it a trusted material in advanced chemical research.

In Indonesian laboratories, (R)-(+)-3-Benzyloxy-1,2-propanediol is commonly used in pharmacological and organic chemistry studies. It is a valuable tool for researchers working on the synthesis of bioactive compounds and the understanding of complex chemical reactions. Its application is widespread in academic and industrial research, supporting the development of new drugs and the exploration of asymmetric reaction mechanisms. The compound's versatility and effectiveness make it an essential resource for scientists in the field of chiral synthesis.

TCI brochures (PDF)

Chiral Building Blocks 2025-04-14 · p. 17

Related TCI products

Asymmetric synthesis of optically active compounds for pharmaceutical development due to its chiral structure and stereochemical control.
Research on complex organic reactions requiring precise stereoselectivity for the creation of biologically active molecules.
Development of new drugs through the synthesis of chiral intermediates that are critical for drug efficacy and specificity.
Investigation of stereochemical effects in chemical reactions to better understand reaction mechanisms and improve synthetic strategies.
Support for biomedical research by enabling the synthesis of compounds with specific biological functions and therapeutic potential.

Brand	TCI
CAS number	56552-80-8
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid or liquid, depending on the specific product formulation
Storage	Store in a cool, dry place away from light and moisture

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 to prevent moisture absorption and maintain chemical integrity. For long-term storage, a desiccator may be used to ensure a controlled humidity level. When handling, it is important to use appropriate personal protective equipment such as gloves and safety goggles to avoid skin contact or inhalation. The compound should be kept in a well-ventilated area to minimize exposure risks. Proper labeling of containers is essential to ensure safe handling and prevent accidental use. Always follow standard laboratory safety protocols when working with chiral compounds to ensure a safe and efficient research environment.

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