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Thermo Scientific Chemicals
4-Chloro-2-methoxyphenol, 97%
CAS: 16766-30-6 | C7H7ClO2 | 158.58 g/mol
| 製品番号（カタログ番号） | 数量 |
|---|---|
| A14806.14 または、製品番号A14806-14 | 25 g |
化学物質識別子
CAS16766-30-6
IUPAC Name4-chloro-2-methoxyphenol
Molecular FormulaC7H7ClO2
InChI KeyFVZQMMMRFNURSH-UHFFFAOYSA-N
SMILESCOC1=CC(Cl)=CC=C1O
さらに表示
仕様
スペックシート
スペックシートAssay (GC)≥96.0%
Appearance (Color)Clear colorless to pale yellow
Refractive Index1.5565-1.5615 @ 20?C
FormLiquid
4-Chloro-2-methoxyphenol, is used as an intermediate in pharmaceutical research, pharmaceutical chemicals and reagents. It is also used as an application intermediate. it can be used to produce 4-Chloro-2-methoxy-6-nitrophenol.
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.
Applications
4-Chloro-2-methoxyphenol, is used as an intermediate in pharmaceutical research, pharmaceutical chemicals and reagents. It is also used as an application intermediate. it can be used to produce 4-Chloro-2-methoxy-6-nitrophenol.
Solubility
It is slightly soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from strong oxidizing agents, strong bases.
4-Chloro-2-methoxyphenol, is used as an intermediate in pharmaceutical research, pharmaceutical chemicals and reagents. It is also used as an application intermediate. it can be used to produce 4-Chloro-2-methoxy-6-nitrophenol.
Solubility
It is slightly soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from strong oxidizing agents, strong bases.
RUO – Research Use Only
General References:
- James T. Traxler. A novel synthesis of 2H-1,3-benzoxathiol-2-ones. J. Org. Chem. 1979, 44, (26), 4971-4973.
- RA Larson .; AL Rockwell. Chloroform and chlorophenol production by decarboxylation of natural acids during aqueous chlorination. Environmental Science & Technology. 1979 13, (3), 325-329.