| Weight | 166.176 g/mol |
|---|---|
| Formula | C9H10O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
4-(hydroxymethyl)phenyl acetate (6309-46-2)
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- (R)-4-Hydroxymethyl-2-phenyl-4,5-dihydrooxazol-4-ylmethyl acetate : chiral building block for the synthesis of optically active -substituted -amino acid derivatives (Tetrahedron, 2006)
- Practical synthesis of a key intermediate for lactacystin from (R)-4-hydroxymethyl-2-phenyl-4,5-dihydrooxazol-4-ylmethyl acetate. (Chemical & Pharmaceutical Bulletin, 2008)
- ChemInform Abstract: Practical Synthesis of a Key Intermediate for Lactacystin from (R)4Hydroxymethyl2phenyl4,5dihydrooxazol4ylmethyl Acetate. (ChemInform, 2008)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(=O)OC1=CC=C(C=C1)CO
-
InChIKeyFKMVNGWJGSSDCF-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Similar Compounds
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51503-08-3
(51503-08-3)
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876-33-5
(876-33-5)
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(18800-34-5)
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(1205-91-0)
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(33901-44-9)
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4-Isobutoxybenzoic acid
(30762-00-6)
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4-Butoxybenzoic acid
(1498-96-0)
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4-(TERT-BUTOXY)BENZOIC ACID
(13205-47-5)
1 alternate name
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(3319-15-1)
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(836-43-1)
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26583-58-4
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(68564-43-2)
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phenyl 2-chloroacetate
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methyl 4-(2-bromoethoxy)benzoate
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(4-cyanophenoxy)acetic acid
(1878-82-6)
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2186-92-7
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4-Benzyloxybenzaldehyde
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4-Ethoxyphenylacetic acid
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N-ethyl-2-(4-methylphenoxy)ethanamine
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4-(hydroxymethyl)phenyl acetate
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