(S)-4-Benzyloxy-1,2-butanediol TCI B2900

Chemical Identity

CAS No.: 69985-32-6
PubChem: CID 9794180·SID 87560102
Formula: C11H16O3
Molecular weight: 196.24 g/mol
Purity: >95.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-4-phenylmethoxybutane-1,2-diol
SMILES: C1=CC=C(C=C1)COCC[C@@H](CO)O
InChIKey: TVRPDIKPMQUOSL-NSHDSACASA-N

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(4-Benzyloxy-1,2-butanediol) is a chemical compound widely used in organic synthesis reactions, particularly in the field of asymmetric synthesis. This compound plays a crucial role in laboratories where the creation of chiral molecules is essential. Its complex structure, featuring two hydroxyl groups on a butanediol chain and a benzyloxy group, makes it a versatile building block for synthesizing compounds with specific stereochemistry. Due to its reactivity and specificity, it is highly valued in organic chemistry research, especially when precise control over molecular configuration is required.

The compound's reactivity in nucleophilic and substitution reactions, along with its stability under certain conditions, makes it a preferred choice for synthetic chemists. Its ability to participate in various chemical transformations while maintaining its chiral integrity is a key factor in its popularity. Additionally, its solubility in organic solvents simplifies its handling and application in laboratory settings. These properties ensure that it remains a reliable and effective tool in the synthesis of complex organic molecules.

In Indonesian laboratories, (4-Benzyloxy-1,2-butanediol) is commonly used in organic chemistry research, particularly in asymmetric synthesis projects. It supports the development of chiral compounds, which are essential in pharmaceutical and fine chemical industries. Its availability and chemical properties make it a standard material for researchers working on stereoselective reactions and chiral molecule synthesis.

TCI brochures (PDF)

Chiral Building Blocks 2025-04-14 · p. 16

Related TCI products

Asymmetric Synthesis: This compound is ideal for creating chiral molecules due to its stereochemical properties, making it a key reagent in stereoselective reactions.
Organic Chemistry Research: It supports the development of complex organic structures, particularly in studies requiring controlled stereochemistry.
Chiral Building Block Applications: Its structural versatility allows it to serve as a foundational element in the synthesis of various chiral compounds.
Pharmaceutical Development: It is used in the synthesis of pharmaceutical intermediates where precise stereochemistry is essential.
Synthetic Chemistry Projects: Its reactivity and solubility make it suitable for a wide range of chemical transformations in laboratory settings.

Brand	TCI
CAS number	69985-32-6
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Liquid or crystalline, depending on the specific 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 light and moisture. It is recommended to use airtight containers to prevent exposure to air and moisture, which may affect its chemical stability. Laboratory personnel should handle it with care, using appropriate personal protective equipment such as gloves and safety goggles. Due to its reactivity, it should be kept in a secure location to avoid accidental exposure. Proper labeling and storage conditions are essential to maintain its effectiveness and ensure safe handling in laboratory environments.

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