(S)-(+)-1,1'-Binaphthyl-2,2'-diyl Hydrogen Phosphate TCI B1144

Chemical Identity

CAS No.: 35193-64-7
PubChem: CID 99589·SID 87564085
Formula: C20H13O4P
Molecular weight: 348.3 g/mol
Purity: >97.0%(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 13-hydroxy-12,14-dioxa-13lambda5-phosphapentacyclo[13.8.0.02,11.03,8.018,23]tricosa-1(15),2(11),3,5,7,9,16,18,20,22-decaene 13-oxide
SMILES: C1=CC=C2C(=C1)C=CC3=C2C4=C(C=CC5=CC=CC=C54)OP(=O)(O3)O
InChIKey: JEHUZVBIUCAMRZ-UHFFFAOYSA-N

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(S)-(+)-1,1'-Binaphthyl-2,2'-diyl Hydrogen Phosphate is a chiral compound widely used in asymmetric synthesis. This material serves as a key chiral building block in laboratories, enabling the creation of complex molecules with precise stereochemistry. Its role is critical in the development of pharmaceuticals and organic compounds where stereochemical control is essential. As a chiral reagent, it supports the synthesis of molecules with specific biological activities, making it a valuable asset in research and development settings.

The compound's unique chiral structure and polar nature make it a preferred choice for asymmetric reactions. Its ability to act as a catalyst or reagent in stereoselective processes enhances the efficiency and specificity of chemical syntheses. Additionally, its solubility in certain organic solvents facilitates purification and isolation steps in laboratory workflows. These properties contribute to its widespread use in both academic and industrial research environments.

In Indonesian laboratories, this compound is commonly utilized in pharmaceutical and organic chemistry research. It supports the development of new drugs and specialty chemicals by providing precise stereochemical control. Its application is particularly relevant in institutions focused on medicinal chemistry, where the synthesis of chiral compounds is a core research activity. Researchers rely on its reliability and performance in achieving desired molecular structures.

TCI brochures (PDF)

Asymmetric Organocatalysts 2025-06-12 · p. 10
Chiral Auxiliaries and Optical Resolving Agents 2025-06-17 · p. 7
Asymmetric Synthesis 2026-03-18 · p. 3
Ligands 2025-12-01 · p. 4

Related TCI products

Asymmetric synthesis is a key application where this compound enables the creation of chiral molecules with high enantiomeric purity.
Pharmaceutical research benefits from its use in the development of drugs requiring precise stereochemical control for efficacy and safety.
Organic chemistry experiments utilize it as a chiral building block for constructing complex molecular frameworks.
Chiral catalysis applications rely on its ability to influence reaction pathways and enhance stereoselectivity.
Analytical chemistry uses it as a reference standard for assessing stereochemical outcomes in synthetic processes.

Brand	TCI
CAS number	35193-64-7
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid
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 to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its stability. Due to its polar nature, it should be handled with care to avoid contamination. In laboratory settings, proper personal protective equipment should be worn when handling it to ensure safety. It is important to store it separately from incompatible substances to prevent any adverse reactions. Regular monitoring of storage conditions is advised to ensure optimal preservation of the compound's properties.

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