Lot numbers can be found on the outside label of a product:
1-(4-Chlorophenyl)-1-phenylethanol
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CAS No. 59767-24-7
- Cat. No. CS-0154094
- Purity≥97%
- MDL No.MFCD09743490
*For research and further manufacturing use only, not for direct human use.
Structure of 59767-24-7
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General Information
- CAS No. 59767-24-7
- Cat. No. CS-0154094
- Purity ≥97%
- MDL No. MFCD09743490
- Storage Store at room temperature
- Shipping Room temperature in continental US; may vary elsewhere.
- Molecular Formula C₁₄H₁₃ClO
- Molecular Weight 232.71
- Synonym(s) α-Methyl-α-phenyl-4-chlorobenzenemethanol
- SMILES CC(C1=CC=CC=C1)(C2=CC=C(C=C2)Cl)O
Description
Dapsone is an antibacterial drug, belongs to a class of compounds known as sulfones. It acts by inhibiting the synthesis of dihydrofolic acid through competition with para-aminobenzoate for the active site of dihydropteroate synthetase, thereby inhibiting the growth of microorganisms that are dependent on endogenous folic acid synthesis. It is used in primary treatment of dermatitis herpetiformis and in combination with other drugs to treat leprosy.Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.Dapsone may be used as a pharmaceutical reference standard for the determination of the analyte in bulk drug and pharmaceutical formulations by chromatography.
Application
1-(4-Chlorophenyl)-1-phenylethanol serves as a versatile chiral building block in synthetic organic chemistry, enabling efficient access to pharmaceutically relevant arylalkyl scaffolds. Its bench-stable, crystalline nature facilitates straightforward purification and handling, while the pendant phenyl and para-chlorophenyl groups provide orthogonal functionalization sites. The molecule participates reliably in standard transformations such as oxidation, reduction, and coupling reactions, supporting diverse applications in medicinal chemistry and process development.
Synthesis
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Route1
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108-86-1 -
99-91-2
- ~25%
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In-stock
59767-24-7
References
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AUSPEX PHARMACEUTICALS, INC. Patent: US2009/203763 A1, 2009 ; Location in patent: Page/Page column 35 ; US 20090203763 A1
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Route2
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1118917-34-2
- ~75%
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In-stock
59767-24-7
References
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Clayden, Jonathan; Farnaby, William; Grainger, Damian M.; Hennecke, Ulrich; Mancinelli, Michele; Tetlow, Daniel J.; Hillier, Ian H.; Vincent, Mark A. Journal of the American Chemical Society, 2009 , vol. 131, # 10 p. 3410 - 3411
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Route3
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99-91-2
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100-58-3
- ~91%
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In-stock
59767-24-7
References
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Zhou, Shuangliu; Wu, Kuo-Hui; Chen, Chien-An; Gau, Han-Mou Journal of Organic Chemistry, 2009 , vol. 74, # 9 p. 3500 - 3505
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Safety Information
Download SDS|
GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H319
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Precautionary Statements : P264-P270-P280-P301+P310-P305+P351+P338-P330-P337+P313-P501
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Quality Control
Computational Chemistry Data
- TPSA 20.23
- LogP 3.5958
- H_Acceptors 1
- H_Donors 1
- Rotatable_Bonds 2
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Key Words
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