| Weight | 170.595 g/mol |
|---|---|
| Formula | C8H7ClO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
4-Methoxybenzoyl chloride (100-07-2)
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- Chlorination of 4-methoxybenzoyl chloride (1981)
- Fries rearrangement: scalable synthesis of key fluoro building blocks 3-fluoro-4-methoxybenzoyl chloride and 1,2-diethoxy-3-fluorobenzene (Tetrahedron Letters, 2014)
- Industrial preparation method of 2,4,5-trifluoro-3-methoxybenzoyl chloride (2013)
- Scheme 1, Synthesis of ML400, conditions: a. 4-Methoxybenzoyl chloride, DIPEA, DCM, 0C to RT, overnight (80%); b. t-BuOK, t-BuOH, 75C, overnight (84%); c. POCl3, 90C, overnight (61%); d. 3-(Piperidin-1-yl)propan-1-amine, t-BuOK 10%, Dry DMA, 135C, overnight, nitrogen atmosphere (57%) (2015)
- ChemInform Abstract: Fries Rearrangement: Scalable Synthesis of Key Fluoro Building Blocks 3Fluoro4methoxybenzoyl Chloride (IV) and 1,2Diethoxy3fluorobenzene (V). (ChemInform, 2014)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=CC=C(C=C1)C(=O)Cl
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InChIKeyMXMOTZIXVICDSD-UHFFFAOYSA-N
- Pubchem - 4-Methoxybenzoyl chloride
- Wikipedia - p-anisoyl chloride
Anisoyl chloride (also called methoxybenzoyl chloride) is an acyl halide, specifically an aromatic acyl chloride, and may be formed from anisic acid by replacing a hydroxyl group of the carboxylic acid with a chloride group. There are three isomers: the ortho-, meta-, and para- forms. Their structures differ in the arene substitution patternthe location of the methoxy group on the ring as compared to the acyl halide.
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