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CAS 86990-91-2

(R)-4-Benzyloxy-1,2-butanediol TCI B2899

(R)-4-Benzyloxy-1,2-butanediol TCI B2899

Chemical Identity

CAS No.
86990-91-2
PubChem
CID 10910454·SID 87560101
Formula
C11H16O3
Molecular weight
196.24 g/mol
Purity
>97.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(2R)-4-phenylmethoxybutane-1,2-diol
SMILES
C1=CC=C(C=C1)COCC[C@H](CO)O
InChIKey
TVRPDIKPMQUOSL-LLVKDONJSA-N
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(R)-4-Benzyloxy-1,2-butanediol is a chiral building block widely used in asymmetric synthesis to construct complex molecular structures. This compound plays a critical role in laboratories where the development of chiral compounds is essential. Its unique stereochemistry allows chemists to control the spatial arrangement of atoms during synthesis, leading to the creation of molecules with specific biological activities. As a key reagent in organic chemistry, it supports the design of pharmaceuticals and other specialized chemical products.

The compound's molecular structure features a benzyloxy group at the fourth carbon and hydroxyl groups at positions one and two, which contribute to its reactivity and selectivity in chemical reactions. The presence of the benzyloxy group also enhances its stability during synthetic processes, making it a reliable choice for complex reactions requiring stereoselective control. Its consistent chemical and physical properties ensure predictable behavior across different experimental conditions, facilitating reproducibility in research settings.

In Indonesian laboratories, (R)-4-Benzyloxy-1,2-butanediol is commonly used in scientific research and chemical product development. Researchers in educational institutions and research organizations rely on this compound to advance their studies in organic synthesis and pharmacology. Its availability and performance make it a valuable tool for both academic and industrial applications in the chemical sciences.

TCI brochures (PDF)

  • Asymmetric synthesis is a key application where this compound is used to create chiral molecules with specific stereochemical configurations, enabling the development of pharmaceuticals and bioactive compounds.
  • Organic chemistry research benefits from its structural versatility, allowing chemists to explore new reaction pathways and functional group transformations in complex molecules.
  • Pharmaceutical development relies on this compound to synthesize drug candidates with desired biological activities, improving the efficiency of drug discovery processes.
  • Chiral compound synthesis requires precise stereocontrol, and this material provides the necessary building block for creating enantiomerically pure substances.
  • Industrial chemical production uses this compound to manufacture specialty chemicals with defined stereochemistry, supporting the development of advanced materials and formulations.

Brand TCI
CAS number 86990-91-2
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 variant
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 contamination. Proper ventilation is essential when handling the material to minimize exposure to vapors. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, to ensure safe handling. The compound is typically stored in a designated chemical storage cabinet to maintain a secure and organized workspace. Regular monitoring of storage conditions ensures the integrity and stability of the material over time.

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