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Thermo Scientific Chemicals
4-Chlorobenzyl alcohol, 99%
CAS: 873-76-7 | C7H7ClO | 142.582 g/mol
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化學識別
CAS873-76-7
IUPAC Name(4-chlorophenyl)methanol
Molecular FormulaC7H7ClO
InChI KeyPTHGDVCPCZKZKR-UHFFFAOYSA-N
SMILESOCC1=CC=C(Cl)C=C1
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規格
規格表
規格表Appearance (Color)White to pale cream
Identification (FTIR)Conforms
Assay (GC)≥98.5%
Melting Point (clear melt)69.0-75.0?C
FormCrystals or powder or crystalline powder or flakes
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Suitable for battery materials development.
Applications
4-Chlorobenzyl alcohol acts as a reagent for the protection of carboxyl groups as their 4-chlorobenzyl esters, more stable to acid than the corresponding benzyl esters. It is used as solvent in paint stripper and waterborne coatings. It acts as curing agent. It is also used in pharmaceuticals, cosmetics, preservatives, and flavoring & fragrance agents.
Solubility
Soluble in water (2.5 mg/ml at 20°C), and methanol.
Notes
Store in a cool, dry, well-ventilated area away from incompatible substances such as oxidizing agents.
4-Chlorobenzyl alcohol acts as a reagent for the protection of carboxyl groups as their 4-chlorobenzyl esters, more stable to acid than the corresponding benzyl esters. It is used as solvent in paint stripper and waterborne coatings. It acts as curing agent. It is also used in pharmaceuticals, cosmetics, preservatives, and flavoring & fragrance agents.
Solubility
Soluble in water (2.5 mg/ml at 20°C), and methanol.
Notes
Store in a cool, dry, well-ventilated area away from incompatible substances such as oxidizing agents.
RUO – Research Use Only
General References:
- Kenji Matsuno; Kazushige Takai; Yoshinobu Isaka; Yuka Unno; Masayuki Sato; Osamu Takikawa; Akira Asai. S-Benzylisothiourea derivatives as small-molecule inhibitors of indoleamine-2,3-dioxygenase. Bioorganic & Medicinal Chemistry Letters.2010, 20 (17), 5126-5129.
- Reagent for the protection of carboxyl groups as their 4-chlorobenzyl esters, more stable to acid than the corresponding benzyl esters: J. Org. Chem., 41, 2579 (1976).