| Identification | More | [Name]
Methyl 6-bromo-2-naphthoate | [CAS]
33626-98-1 | [Synonyms]
6-BROMO-2-NAPHTHALENECARBOXYLIC ACID METHYL ESTER
6-BROMO-2-NAPHTHOIC ACID METHYL ESTER
METHYL 6-BROMO-2-NAPHTHALENECARBOXYLATE
METHYL 6-BROMO-2-NAPHTHOATE
6-Bromo-2-Naphtoic Acid Methyl Ester
2-Bromo-6-naphthoic acid methylester
Methyl-6-bromo-2-naphtoate
6-BROMO-2-NAPHTHOIC AICD
6-BROMO-2-NAPHTHOIC AICD, METHYL ESTER
2-Naphthoic acid, 6-bromo, methyl ester
6-Bromonaphthalene-2-carboxylic acid methyl ester | [EINECS(EC#)]
608-896-0 | [Molecular Formula]
C12H9BrO2 | [MDL Number]
MFCD00100408 | [Molecular Weight]
265.1 | [MOL File]
33626-98-1.mol |
| Chemical Properties | Back Directory | [Appearance]
Pale yellow or light brown powder | [Melting point ]
123-126 °C (lit.) | [Boiling point ]
357.0±15.0 °C(Predicted) | [density ]
1.492±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
Chloroform (Slightly), DMSO (Slightly) | [form ]
Crystalline Powder | [color ]
Off-white to cream or light brown | [BRN ]
2578943 | [InChIKey]
JEUBRLPXJZOGPX-UHFFFAOYSA-N | [CAS DataBase Reference]
33626-98-1(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
C | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R34:Causes burns. | [Safety Statements ]
S24/25:Avoid contact with skin and eyes .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S27:Take off immediately all contaminated clothing .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [HS Code ]
29163990 |
| Hazard Information | Back Directory | [Chemical Properties]
Pale yellow or light brown powder | [Uses]
Methyl 6-Bromo-2-napthoate is used in the synthesis of Adapalene, a retinoid specific for RARβ and RARγ receptors. | [General Description]
Methyl 6-bromo-2-naphthoate undergoes aromatic Finkelstein reaction followed by hydrolysis to afford 6-iodo-2-naphthoic acid. |
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