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| IUPAC Name: | (2-bromophenyl)methanol |
| Description: | 2-Bromobenzyl Alcohol acts as a reagent for the synthesis of alkoxy tetrasubstituted chiral amino acids via three-component reaction of (diazo)oxindoles, alcohols and benzhydrylimino ester involving enantioselective trapping of oxonium ylides by benzhydrylimino ester. Also acts as a reagent for the preparation of orally active and liver-targeted prodrug of 5-fluoro-2'-deoxyuridine for treatment of hepatocellular carcinoma. |
| Molecular Weight: | 187.03 |
| Molecular Formula: | C7H7BrO |
| Canonical SMILES: | C1=CC=C(C(=C1)CO)Br |
| InChI: | InChI=1S/C7H7BrO/c8-7-4-2-1-3-6(7)5-9/h1-4,9H,5H2 |
| InChI Key: | IOWGHQGLUMEZKG-UHFFFAOYSA-N |
| Boiling Point: | 261.8 ℃ at 760 mmHg |
| Purity: | 98 % |
| Density: | 1.565 g/cm3 |
| Appearance: | White to beige crystalline powder or needles |
| MDL: | MFCD00004600 |
| LogP: | 1.94140 |
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Oxygen Compounds
2-(6,8-difluoro-1,2,3,4-tetrahydro-naphthalen-2-ylamino)-pentanoic acid methyl ester
2,2-Difluoro-N-(4-methoxy-3-(methoxymethyl)benzyl)ethanamine
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